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. 2023 Nov 20;13(48):33566–33587. doi: 10.1039/d3ra06560j

Recyclable mesalamine-functionalized magnetic nanoparticles (mesalamine/GPTMS@SiO2@Fe3O4) for tandem Knoevenagel–Michael cyclocondensation: grinding technique for the synthesis of biologically active 2-amino-4H-benzo[b]pyran derivatives†

Mahdiyeh Partovi a, Sobhan Rezayati a, Ali Ramazani a,b,✉, Yavar Ahmadi c, Hooman Taherkhani a
PMCID: PMC10658220  PMID: 38020042

Abstract

In the present study, mesalamine-functionalized on magnetic nanoparticles (mesalamine/GPTMS@SiO2@Fe3O4) is fabricated as an efficient and magnetically recoverable nanocatalyst. The as-prepared nanocatalyst was successfully synthesized in three steps using a convenient and low-cost method via modification of the surface of Fe3O4 nanoparticles with silica and GPTMS, respectively, to afford GPTMS@SiO2@Fe3O4. Finally, treatment with mesalamine as a powerful antioxidant generates the final nanocatalyst. Then, its structure was characterized by FT-IR, SEM, TEM, EDX, XRD, BET, VSM, and TGA techniques. The average size was found to be approximately 38 nm using TEM analysis and the average crystallite size was found to be approximately 27.02 nm using XRD analysis. In particular, the synthesized nanocatalyst exhibited strong thermal stability up to 400 °C and high magnetization properties. The activity of the synthesized nanocatalyst was evaluated in the tandem Knoevenagel–Michael cyclocondensation of various aromatic aldehydes, dimedone and malononitrile under a dry grinding method at room temperature to provide biologically active 2-amino-4H-benzo[b]pyran derivatives products in a short time with good yields. The presented procedure offers several advantages including gram-scale synthesis, good green chemistry metrics (GCM), easy fabrication of the catalyst, atom economy (AE), no use of column chromatography, and avoiding the generation of toxic materials. Furthermore, the nanocatalyst can be reused for 8 cycles with no loss of performance by using an external magnet.

Mesalamine-functionalized on magnetic nanoparticles (mesalamine/GPTMS@SiO2@Fe3O4) is synthesized and characterized as an efficient and magnetically recoverable nanocatalyst for the synthesis of biologically active 2-amino-4H-benzo[b]pyran derivatives products via grinding method.graphic file with name d3ra06560j-ga.jpg

Introduction

Due to an increased awareness of the harmful effects of toxic chemical waste and by-products generated through chemical processes on living species, human health and the environment, environmental policies regarding these processes have become much more strict.1 As a result, a variety of regulatory bodies have requested the use of synthetic strategies adhering to green chemistry protocols over conventional synthetic methods in chemical industries. Efficient and green catalysts, which reduce toxic waste, pressure, temperature and by-products, have been found to be of great importance among a variety of aspects for development in chemical processes. Hence, one of the most important challenges for chemists is the design and fabrication of sustainable catalysts to replace conventional, polluting and toxic catalysts. According to the guidelines of green chemistry, a sustainable catalyst for any chemical process must have several advantages such as environmental friendliness, high activity, high stability, efficiency, selectivity, recyclability and reusability.2

Based on the reaction phase, catalysts can be classified into two types: (i) heterogeneous and (ii) homogeneous catalysts. The advantages of homogeneous catalysts are conversion rate, mild conditions, improved yield, increased selectivity, and minimized side reactions. Additionally, this class of catalysts is able to increase the speed of reaction and lead to high turnover numbers (TON). However, their greatest disadvantages are corrosion problems and the ability to recycle and reuse. From an economic and environmental standpoint, chemical processes derived from heterogeneous catalysts are not compatible with the principles of green chemistry. Hence, to avoid these limitations and reduce the gap between heterogeneous and homogeneous catalysis, researchers in this field are focused on nanomaterials as a suitable alternative for catalytic systems.

Nanomaterials are materials that have an average size in the range of 1 to 100 nm. Recently, nanotechnology has received increasing attention in various fields such as wastewater management,3 biology and medicine,4 carbon nanotubes,5 food and nutraceuticals,6 fabrics and textiles,7 biotechnology,8 automobiles,9 and therapeutics and environmental applications.10 Among nanomaterials, magnetic nanoparticles (MNPs) especially Fe3O4 have gained significant attention in the development of new synthetic strategies. These particles are useful and have many applications in various areas such as drug delivery systems, information saving, high specific surface area, sensors, biomedicine, catalysis, targeted gene therapy, magnetic resonance imaging (MRI), and electrical and magnetic characteristics.11

Nanoparticles are not used directly due to their limitations such as unnecessary interactions, toxicity and hydrophobicity. To solve this problem, intermediaries are used as shells or layers. Hence, various layers (inorganic and organic materials) such as metals, silica, biomolecules, polymers, etc. have been used for functionalization and modification of the surface of MNPs. Among these layers, silica as a shell has become one of the most widely used due to its thermal stability, low toxicity, high specific surface area, easy catalyst separation by a magnetic field and so on. In addition, silica, by protecting the core, prevents oxidation, agglomeration and sintering. On the other hand, it also provides a range of different functional groups on the surface, enhancing the performance of the catalyst.12 Thus, the design and synthesis of core–shell magnetic nanocatalysts is one of the most effective strategies in catalysis science for chemical processes.13

Given the need for high energy input and environmental issues in carrying out chemical transformations, using low-cost and time-efficient methods is crucial. The most serious polluting steps in a chemical reaction are the product purification and reaction processes because a large amount of solvent is consumed in both steps. Mechanochemical solvent-free reactions have emerged as suitable and important procedures in both academic and industrial chemistry. This technique is carried out using external mechanical energy for grinding two solids via a shaker, ball-mill or a mortar-and-pestle and is an important alternative method in solution chemistry. Mechanochemistry as a simple operating technique has several notable advantages such as low energy consumption, no need for solvents or volatile organic compounds, and high yields.14 Recently, various compounds and materials (organic and inorganic) such as composites, cocrystals, alloys, metal–organic frameworks, and pharmaceuticals have been synthesized by mechanochemical routes.15 A pestle and mortar can be used for grinding, providing an efficient mechanochemical method, which is used for the synthesis of chemical compounds.16

Mesalamine, also known as 5-aminosalicylic acid (5-ASA), is a powerful antioxidant, which can boost the activity of peroxisome proliferator-activated receptor γ in the intestines. 5-ASA is the main form of treatment for mild to moderate ulcerative colitis. The anti-inflammatory effects of 5-ASA are achieved by reducing the activation of cyclooxygenase,17 inducible nitric oxide synthase,18 interleukin, tumor necrosis factor,19 and a nuclear factor.20 Multiple studies agree that 5-ASA decreases the likelihood of developing cancer in individuals with CUC.21 Additionally, its ability to hinder cell growth and promote cell death in epithelial cells has been observed both in laboratory settings and in living organisms such as mice22 and humans,23 indicating its potential as a treatment against tumors.24

Heterocycle compounds containing oxygen25 and nitrogen26 atoms have been widely used in approved drugs by the United States Food and Drug Administration (USFDA). According to the literature, 59% of drugs approved by USFDA contain nitrogen heterocycles and 311 drugs approved by USFDA contain oxygen heterocycles. Among these compounds, benzopyrans and their derivatives are highly important heterocyclic compounds that are obtained by MCRs. These compounds have attracted much attention due to their wide range of pharmacological and biological activities such as anti-malarial, anti-microbial, anti-HIV, anti-cancer, and anti-inflammatory activities.27 Furthermore, certain compounds within this family have exhibited the potential for treating Alzheimer's and Parkinson's disease.28 Moreover, as depicted in Scheme 1, chromene or 4H-benzo[b]pyran scaffolds have found widespread applications in pharmacologically active substances.29 Additionally, a notable compound belonging to this group is 2-amino-3-cyano-4H-pyran, which is utilized in pigments and cosmetics.30

Scheme 1. Various benzo[b]pyran derivatives possessing important pharmacological and biological properties.

Scheme 1

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Given the importance of these compounds, many catalyst have been developed for the synthesis of 2-amino-3-cyano-4H-pyran such as Fe3O4@SiO2@GPTMS@guanidine,31 Fe3O4@GA@IG,32 Fe3O4@SiO2–NH2@TCT–guanidine,33 boron nitride@Fe3O4,34 montmorillonite,35 GO-Fc@Fe3O4,36 [EMIM][OH],37 nano-SnO2,38 sodium alginate,39 [PEG(mim)2][OH]2,40 iodine,41 cesium fluoride,42 MNPs@Cu,43 DABCO,44 CeCl3·7H2O,45 Fe3O4@GA@IG,46 EDA/(CH2)3@SiO2@Fe3O4,47 NH4H2PO4/Al2O3,48 NiFe2O4@SiO2@H14[NaP5W30O110],49 Ag/Fe3O4@starch,50 per-6-NH2–β-CD,51 Fe3O4@NH2@TCT@HOProCu,52 and molecular iodine.53 Despite some advantages of the reported methods, some of them suffer from various limitations such as high temperatures, reflux conditions, expensive reagents, harsh reaction conditions, extended reaction times, generation of waste materials, tedious work-up procedures, and low yields. To overcome the aforementioned problems, improve the reaction conditions and continue our previous research on the design and synthesis of novel catalysts especially MNPs as a heterogeneous nanocatalyst,54 we synthesized mesalamine-functionalized magnetic nanoparticles with a high surface area as a green heterogeneous nanocatalyst. Then, this nanocatalyst was employed for the synthesis of biologically active 2-amino-3-cyano-4H-pyran products by a solvent-free grinding reaction (Scheme 2).

Scheme 2. Synthesis of 2-amino-4H-benzo[b]pyrans catalyzed by mesalamine/GPTMS@SiO2@Fe3O4.

Scheme 2

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Experimental

Materials and instruments

All materials and solvents used such as aqueous ammonia (25%), dry toluene, ethanol, FeSO4·7H2O, GPTMS, tetraethyl orthosilicate (TEOS), FeCl3, mesalamine, malononitrile, various aromatic aldehydes, and dimedone were provided from Merck and Fluka Companies. FT-IR spectra of the synthesized compounds were confirmed using a PerkinElmer 597 spectrophotometer (University of Zanja, Zanja, Iran). Spectral data of 1H (250 MHz) and 13C NMR (62.5 MHz) using DMSO-d6 were acquired utilizing a Bruker DRX-250 AVANCE instrument (University of Zanja, Zanja, Iran). Elemental analysis of the as-prepared nanocatalyst was evaluated by EDX analysis with specifications FESEM TESCAN MIRA II (Beam Gostar Taban, Tehran, Iran). The magnetic properties of the as-prepared nanocatalyst were evaluated by VSM analysis (Beam Gostar Taban, Tehran, Iran). The crystalline structure of the as-prepared nanocatalyst was evaluated by XRD analysis (Beam Gostar Taban, Tehran, Iran). TEM images with specifications Zeiss EM10C operating at 80 kV TEM were used to determine the morphology of the as-prepared nanocatalyst.

Synthesis of Fe3O4

A co-precipitation procedure was utilized for the synthesis of Fe3O4. To generate Fe3O4, 0.97 g of iron(iii) chloride and 0.9 g of iron(ii) sulfate heptahydrate were added to a solution of distilled H2O (120 mL) under N2 gas at 80 °C. Then, 120 mL of aqueous ammonia solution (1.5 M) was added dropwise to the previous mixture under stirring. In the following step, the contents of the reaction mixture under N2 gas were stirred for 60 min. The produced black Fe3O4 nanoparticles were collected using an external magnet and washed several times with distilled H2O and EtOH, followed by drying at room temperature for 24 h.55

Synthesis of SiO2@Fe3O4

1 g of the produced black Fe3O4 nanoparticles was dispersed in 100 mL of ethanol 96% for 20 min. 2 mL tetraethyl orthosilicate (TEOS) and 2 mL of NH4OH 25% were added and the mixture was stirred for 12 h under N2 gas. The produced black Fe3O4@SiO2 nanoparticles were collected using an external magnet and washed several times with distilled H2O and EtOH followed by drying at 40 °C for 24 h.55

Synthesis of GPTMS@SiO2@Fe3O4

1 g of the produced SiO2@Fe3O4 nanoparticles was dispersed in 100 mL of dry toluene for 20 min. 10 mmol GPTMS was added and the mixture was stirred for 8 h at 80 °C under N2 gas. The produced black GPTMS@SiO2@Fe3O4 nanoparticles were collected using an external magnet and washed twice with dry toluene to remove the unreacted GPTMS, followed by drying at room temperature for 24 h.55

Synthesis of mesalamine/GPTMS@SiO2@Fe3O4

1 g of produced GPTMS@SiO2@Fe3O4 nanoparticles was dispersed in 100 mL of ethanol 96% for 20 min. In the following, 10 mmol mesalamine was added and the mixture was stirred under reflux conditions and N2 gas for 24 h. The produced brown mesalamine/GPTMS@SiO2@Fe3O4 nanoparticles were collected using an external magnet and washed several times with EtOH to remove unreacted mesalamine, followed by drying at room temperature for 24 h.

Typical procedure for the synthesis of 2-amino-4H-benzo[b]pyrans

Various aromatic aldehydes (1 mmol), dimedone (1 mmol), malononitrile (1 mmol), and nanocatalyst (0.07 g) were added to a mortar and ground at room temperature. The progress of the reaction was monitored by TLC. After the reaction, the thick paste substance was dissolved with ethanol (2 × 10 mL). Subsequently, the nanocatalyst was recovered from the reaction mixture using a magnetic field. Finally, the crude product was purified by recrystallization from ethanol to obtain the product.

Compound 4b

FT-IR (KBr, cm−1): 3379, 3182, 2958, 2188, 1674, 1589, 1459, 1367, 1215, 1094, 1013, 828, 616, 521. 1H-NMR (250 MHz, DMSO-d6): δ 7.33 (d, 2H, J = 7.5 MHz, Ar–H), 7.19 (d, 2H, J = 8.25 MHz, Ar–H), 7.05 (s, 2H, NH2), 4.65 (s, 1H, C–H), 2.19–2.41 (m, 2H, CH2), 2.02–2.08 (m, 2H, CH2), 1.01 (s, 3H, Me), 0.95 (s, 3H, Me). 13C-NMR (62.5 MHz, DMSO-d6): δ 18.9, 27.3, 28.7, 32.1, 33.1, 38.9, 50.3, 56.4, 56.7, 111.8, 119.5, 128.0, 129.1, 131.8, 132.2, 133.4, 141.1, 159.1, 163.7, 196.0.

Compound 4c

FT-IR (KBr, cm−1): 3396, 3324, 3212, 2960, 2199, 1679, 1604, 1604, 1371, 1214, 1036, 839, 695. 1H-NMR (250 MHz, DMSO-d6): δ 6.91–7.84 (m, 6H, Ar–H, NH2), 4.16 (s, 1H, C–H), 2.10–2.48 (m, 4H, 2CH2), 0.92 (s, 3H, Me), 1.00 (s, 3H, Me). 13C-NMR (62.5 MHz, DMSO-d6): δ 31.0, 31.7, 32.2, 32.9, 35.6, 47.1, 50.4, 56.5, 114.6, 129.2, 129.9, 131.0, 132.5, 133.1, 158.9, 160.7, 196.6.

Compound 4e

FT-IR (KBr, cm−1): 3405, 3321, 3185, 2963, 2192, 1682, 1652, 1631, 1594, 1521, 1349, 1215, 1033, 827. 1H-NMR (250 MHz, DMSO-d6): δ 7.15–8.25 (m, 6H, Ar–H, NH2), 4.34 (s, 1H, C–H), 3.03–3.39 (m, 2H, CH2), 2.06–2.20 (m, 2H, CH2), 1.13 (s, 3H, Me), 1.01 (s, 3H, Me). 13C-NMR (62.5 MHz, DMSO-d6): δ 22.9, 24.2, 27.7, 31.8, 45.8, 52.0, 53.1, 114.7, 115.3, 124.3, 128.3, 146.2, 154.5, 159.0.

Compound 4f

FT-IR (KBr, cm−1): 3383, 3316, 3208, 3026, 2963, 2192, 1682, 1654, 1605, 1510, 1410, 1368, 1250, 1214, 1036, 845, 770. 1H-NMR (250 MHz, DMSO-d6): δ 6.93–8.42 (m, 6H, Ar–H, NH2), 4.11 (s, 1H, C–H), 2.21 (s, 3H, Me), 2.36–2.46 (m, 4H, 2CH2), 1.00 (s, 3H, Me), 0.93 (s, 3H, Me). 13C-NMR (62.5 MHz, DMSO-d6): δ 14.5, 22.8, 24.2, 27.7, 31.1, 45.9, 52.9, 53.6, 108.2, 115.5, 125.5, 127.1, 140.1, 154.4, 158.6, 191.6.

Compound 4h

FT-IR (KBr, cm−1): 3431, 2230, 1635, 1595, 1507, 1416, 1367, 1304, 1244, 1165, 838, 616, 529, 438. 1H-NMR (250 MHz, DMSO-d6): δ 6.98–8.50 (m, 6H, Ar–H, NH2), 4.17 (s, 1H, C–H), 2.19–2.51 (m, 2H, CH2), 2.04–2.10 (m, 2H, CH2), 1.0 (s, 3H, Me), 0.92 (s, 3H, Me). 13C-NMR (62.5 MHz, DMSO-d6): δ 27.3, 28.2, 28.7, 32.2, 35.3, 47.1, 50.4, 115.2, 115.6, 117.2, 117.5, 129.5, 134.0, 141.3, 160.6, 162.9, 196.1.

Compound 4m

FT-IR (KBr, cm−1): 3396, 3323, 3212, 2959, 2190, 1682, 1654, 1604, 1489, 1366, 1250, 1214, 1034, 847, 561. 1H-NMR (250 MHz, DMSO-d6): δ 7.13–7.90 (m, 4H, Ar–H), 7.02 (s, 2H, NH2), 4.32 (s, 1H, CH), 2.09–2.47 (m, 4H, 2CH2), 1.00 (s, 3H, Me), 0.98 (s, 3H, Me). 13C-NMR (62.5 MHz, DMSO-d6): δ 26.6, 28.3, 29.5, 32.5, 35.3, 50.7, 55.2, 59.4, 102.8, 104.3, 110.6, 113.6, 128.8, 140.4, 145.0, 149.7, 157.7, 194.7.

Compound 4o

FT-IR (KBr, cm−1): 3531, 3364, 3158, 2961, 2191, 1721, 1685, 1609, 1475, 1368, 1216, 1042, 861, 563. 1H-NMR (250 MHz, DMSO-d6): δ 7.21–7.41 (m, 3H, Ar–H), 7.07 (s, 2H, NH2), 5.19 (s, 1H, CH), 2.06–2.51 (m, 4H, 2CH2), 0.98 (s, 6H, 2Me). 13C-NMR (62.5 MHz, DMSO-d6): δ 18.9, 27.3, 28.9, 31.9, 32.7, 50.3, 54.0, 56.4, 110.4, 119.4, 128.9, 129.4, 130.6, 134.6, 136.3, 136.7, 159.9, 164.1, 196.1.

Results and discussion

The as-prepared magnetic nanocatalyst is prepared simply using a multistep procedure. To do this, firstly, Fe3O4 nanoparticles are prepared at room temperature. In the second step, the Fe3O4 nanoparticles were covered with TEOS under N2 at room temperature, and in sequence, they were coated with GPTMS by heating at reflux conditions to give GPTMS@SiO2@Fe3O4. Finally, the nanoparticles synthesized in the previous step were treated with mesalamine to give mesalamine/GPTMS@SiO2@Fe3O4 with high activity and a schematic for the synthesis of all the stages of the nanocatalyst is indicated in Scheme 3. Various techniques such as FT-IR, SEM, TEM, EDX, XRD, BET, VSM, and TGA were used to ensure the identification of the properties and the correct synthesis steps of the synthesized nanocatalyst.

Scheme 3. Preparation of the mesalamine/GPTMS@SiO2@Fe3O4 magnetic nanoparticles.

Scheme 3

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FT-IR spectroscopy with KBr pellets was performed for identification of the functional groups for the stepwise characterization of the as-prepared nanocatalyst in the range of 4000–400 cm−1. The FT-IR spectra of Fe3O4, SiO2@Fe3O4, GPTMS@SiO2@Fe3O4 and mesalamine/GPTMS@SiO2@Fe3O4 are illustrated in Fig. 1. In Fig. 1a, the broad band near 616 cm−1 corresponds to the Fe–O functional group of Fe3O4 NPs.55 In Fig. 1b, we see the silica-coated Fe3O4 NPs. The peak in the 3459 cm−1 region is due to the O–H group on the SiO2 group. Moreover, the wide absorption peak at about 1096 cm−1 was ascribed to the Si–O group.55 After the reaction between SiO2@Fe3O4 and GPTMS, the corresponding GPTMS@SiO2@Fe3O4 was afforded (Fig. 1c). As expected, curve c indicated the new adsorption peak at 2924 cm−1, which is related to the –CH2 stretching. Also, the adsorption peak appearing near 1208 cm−1 is associated with the C–O of the epoxy, which overlapped with the strong absorption of the bare silica.55 These adsorptions verified the existence of the epoxy group in the structure of catalyst. Finally, Fig. 1d shows the spectrum of mesalamine/GPTMS@SiO2@Fe3O4. After covering of mesalamine with GPTMS@SiO2@Fe3O4, new wide signals at 2787–3430 cm−1 and 1646 cm−1 are observed for the hydroxyl and carbonyl groups of the CO2H group. Furthermore, absorption peaks appeared at 1623 cm−1 and 1453 cm−1 which are related to the C Created by potrace 1.16, written by Peter Selinger 2001-2019 C stretching and N–H bending, showing that mesalamine covered GPTMS@SiO2@Fe3O4.

Fig. 1. FT-IR spectra of (a) Fe3O4, (b) SiO2@Fe3O4, (c) GPTMS@SiO2@Fe3O4, and (d) mesalamine/GPTMS@SiO2@Fe3O4 magnetic nanoparticles.

Fig. 1

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XRD analysis was performed to determine the crystallite size, inter-planar distance, Miller indices (h k l), and structural properties of the as-prepared nanocatalyst (Fig. 2). As depicted in Fig. 2, seven peaks at 2θ values of 32.1, 38.1, 45.5, 56.4, 59.7, 65.1, and 74.4 are observed, which can correspond to the diffraction lattice planes (220), (311), (400), (422), (511), (440), and (533), respectively. The obtained results clearly confirmed the cubic structure of Fe3O4, which matched the JCPDS data (JCPDS file no. 01-076-7166). The data reported by Singh et al., Kumar et al. and Cheng et al. also support this result.56 These peaks demonstrated the stability of the Fe3O4 during various stages of the catalyst synthesis. Also, no relevant peak was found for silica, which is due to the amorphous structure of SiO2.56 Moreover, the XRD data such as crystallite size, inter-planar distance, Miller indices (h k l), and peak width of the as-prepared nanocatalyst was calculated for all 7 peaks at the 2θ values, as indicated in Table 1. The result showed that based on Scherrer's formula Inline graphic and Bragg's formula Inline graphic the average crystallite size and average inter-planar distance of the as-prepared nanocatalyst were found to be 27.02 nm and 0.1906 nm.

Fig. 2. XRD patterns of mesalamine/GPTMS@SiO2@Fe3O4.

Fig. 2

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The XRD data for the mesalamine/GPTMS@SiO2@Fe3O4.

Entry 2θ Peak width (FWHM) Miller indices Crystallite size (nm) Inter-planar distance (nm)
h k l
1 32.1 0.1968 1 0 4 41.8 0.2703
2 38.1 0.1968 1 1 0 42.3 0.2519
3 45.5 0.3444 2 0 2 24.8 0.2080
4 56.4 0.2952 1 1 6 30.1 0.1696
5 59.7 0.6888 1 2 2 13.1 0.1601
6 65.1 0.7882 2 1 4 11.8 0.1487
7 74.4 0.3936 2 2 0 25.3 0.1259
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Magnetic properties are one of the most important properties of a catalyst, which lead to its easy and clean recovery from reaction media. For this purpose, VSM analysis was employed for the magnetic properties of (a) Fe3O4 and (b) mesalamine/GPTMS@SiO2@Fe3O4 magnetic nanoparticles, and the results are presented in Fig. 3A. As can be seen, both Fe3O4 and the final catalyst exhibited superparamagnetic properties. Moreover, the saturation magnetization for Fe3O4 and mesalamine/GPTMS@SiO2@Fe3O4 was 33.83 emu g−1 and 17.82 emu g−1, respectively. This decrease in saturation magnetization is due to the coverage of various compounds on the surface of iron oxide. As a result, the as-prepared nanocatalyst shows a good ability as a magnetically recoverable nanocatalyst. Moreover, Fig. 3B shows that the nanoparticle has magnetic properties and responds quickly to the magnetic field and disperses quickly in the absence of the magnetic field.

Fig. 3. (A) Magnetization curves obtained by VSM for Fe3O4 and mesalamine/GPTMS@SiO2@Fe3O4 MNP. (B) Magnetic separation of mesalamine/GPTMS@SiO2@Fe3O4 MNP.

Fig. 3

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To determine the organic functional groups content and thermal stability of the as-prepared nanocatalyst, TGA analysis was carried out over the temperature range of 25 to 800 °C (Fig. 4). As can be seen, the as-prepared nanocatalyst shows three steps of weight loss. Below 100 °C, 200–400, and >400 °C. The initial stage occurs below 100 °C due to the elimination of the adsorbed solvent or water on the trap in the complex used in the synthesis of the catalyst. The second stage occurring at 200–400 °C is attributed to the elimination of the organic linker in the as-prepared nanocatalyst. This result indicated that the core/shell structure has been successfully immobilized with various organic compounds. The third stage occurring at about >400 °C is attributed to the elimination of the mesalamine groups located on the surface of GPTMS@SiO2@Fe3O4.

Fig. 4. TGA analysis for the mesalamine/GPTMS@SiO2@Fe3O4 magnetic nanoparticles.

Fig. 4

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The morphology, particle size and shape of the produced particles such as Fe3O4 and mesalamine/GPTMS@SiO2@Fe3O4 were determined by the FE-SEM technique and the images are depicted in Fig. 5. The FE-SEM image obtained from Fe3O4 indicated that the structure exhibits a particle size of 20.5 nm and a uniform spherical shape (Fig. 5A). Also, the FE-SEM images obtained from mesalamine/GPTMS@SiO2@Fe3O4 indicated that the structure shows a spherical and regular morphology (Fig. 5B and C). It seems that from Fe3O4 to the final catalyst, a significant surface-roughening has occurred. This surface-roughening could be due to certain parameters such as different coatings (silica, GPTMS and mesalamine) on the core. Furthermore, a histogram of the final catalyst indicated an average diameter of approximately 36–46 nm (Fig. 5D).

Fig. 5. FE-SEM images of (A) Fe3O4, (B and C) mesalamine/GPTMS@SiO2@Fe3O4, and (D) a histogram of mesalamine/GPTMS@SiO2@Fe3O4.

Fig. 5

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The core–shell structure and appearance of the produced particles such as Fe3O4 and mesalamine/GPTMS@SiO2@Fe3O4 were determined by a TEM technique and the images are depicted in Fig. 6. The images and histogram clearly show that the nanoparticles were synthesized in nanodimensions. The TEM image of the Fe3O4 nanoparticles indicated that the structure has a particle size of about 25 nm and a uniform spherical shape (Fig. 6A). The TEM image of the mesalamine/GPTMS@SiO2@Fe3O4 nanoparticles indicated that the nanostructure was synthesized with a uniform spherical shape and a core–shell structure (Fig. 6B and C). Besides, Fig. 6C clearly shows that the final catalyst is formed as a shell–core structure. The dark area is related to the core and the light area is related to the shell. Furthermore, a histogram of the final catalyst is shown in Fig. 6D, which shows an average diameter of approximately 34–44 nm.

Fig. 6. TEM images of (A) Fe3O4, (B and C) mesalamine/GPTMS@SiO2@Fe3O4, and (D) a histogram of mesalamine/GPTMS@SiO2@Fe3O4.

Fig. 6

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EDX analysis was applied to identify the elements present in the synthesized nanocatalyst (Fig. 7). Fig. 7 clearly indicates that the synthesized nanocatalyst was composed from C, N, O, Fe, and Si with relative mass percentages of 35.12, 14.87, 35.53, 3.57, and 10.91%, respectively.

Fig. 7. EDX spectra of mesalamine/GPTMS@SiO2@Fe3O4.

Fig. 7

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Fig. 8 provides visual insights into the spatial distribution of the elements within the mesalamine/GPTMS@SiO2@Fe3O4 complex, complementing the EDX analysis. The images reveal a large concentration of Fe and O elements, while the support material displays an even distribution of C, N, and Cu components, indicating a successful blending of various catalyst elements. This suggests that the structure has been well prepared and persists.

Fig. 8. Elemental mapping of mesalamine/GPTMS@SiO2@Fe3O4.

Fig. 8

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Finally, to determine the properties of Fe3O4 and the as-prepared nanocatalyst such as surface area, mean pore diameter, total pore volume, and type of isotherm, BET analysis was performed (Fig. 9). As shown in Fig. 9A, the BET isotherm of the as-prepared nanocatalyst is type IV, which is related to mesoporous materials. Table 2 displays the specific information on the surface area, mean pore diameter, and total pore volume of Fe3O4 and the nanocatalyst prepared in this study. Fe3O4 was synthesized with a small pore diameter of approximately 21.5 nm, while the surface area and total pore volume were measured at 112.36 m2 g−1 and 0.815 cm3 g−1, respectively. Moreover, mesalamine/GPTMS@SiO2@Fe3O4 has a surface area of 55.21 m2 g−1 with mean pore diameter of 29.63 nm and total pore volume of 0.425 cm3 g−1, respectively. Coating different organic compounds, SiO2, GPTMS, and mesalamine onto the surface of Fe3O4 results in a significant reduction in surface area and total pore volume, as indicated by this comparison.

Fig. 9. BET analysis of mesalamine/GPTMS@SiO2@Fe3O4.

Fig. 9

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BET data of Fe3O4 and mesalamine/GPTMS@SiO2@Fe3O4.

Sample Surface area (m2 g−1) Total pore volume (cm3 g−1) Average pore diameter (nm)
Fe3O4 112.36 0.815 21.5
Mesalamine/GPTMS@SiO2@Fe3O4 55.21 0.425 29.63
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After fabrication of the as-prepared nanocatalyst and analyzing its structure through various techniques, we decided on finding an eco-friendly, simple and efficient method for the synthesis of 2-amino-4H-benzo[b]pyran derivatives products in the presence of mesalamine/GPTMS@SiO2@Fe3O4 as an efficient and magnetically recoverable nanocatalyst. For this purpose, a model reaction of benzaldehyde (1 mmol), dimedone (1 mmol) and malononitrile (1 mmol) (liquid, solid, solid) in the presence of mesalamine/GPTMS@SiO2@Fe3O4 under the dry grinding method was tested to give the desired product 4a (Table 3 and Fig. 10). In this reaction optimization to create favorable conditions, a variety of parameters like the effect of solvent, temperature and catalyst amount was evaluated and the obtained results are indicated in Table 3. In the desired product 4a, a favorable result was obtained using 0.07 g of catalyst under a dry grinding method at room temperature (Table 3, entry 8). When the reaction was tested in the absence of a catalyst under grinding conditions or 80 °C, the product 4a yield was traced (Table 3, entries 1 and 2). When mesalamine/GPTMS@SiO2@Fe3O4 was used as a catalyst under grinding conditions at room temperature, good to excellent product yields were observed for 4a (Table 3, entries 3–10). Among various loadings of catalyst (0.005–0.1 g), 0.07 g was found to be the best loading and 4a was formed at 95% yield after 15 min (Table 3, entry 8). When the reaction was conducted with 0.09 and 0.1 g of catalyst, 4a was formed at 90 and 88%, respectively (Table 3, entries 9 and 10). Furthermore, various solvents such as EtOH, EtOH/H2O, H2O, toluene, and chloroform were tested but none of them were not suitable for this reaction (Table 3, entries 11–15). Hence, the reaction of 4a was optimum in the presence of 0.07 g of catalyst under the dry grinding method at room temperature.

Effects of various factors on the synthesis of 4aa.

graphic file with name d3ra06560j-u1.jpg
Entry Nanocatalyst (g) Conditions Solvent (3 mL) Time (min) Yieldb (%)
1 — Grinding, r.t. — 30 Trace
2 — 80 °C — 180 Trace
3 0.005 Grinding, r.t. — 30 25
4 0.007 Grinding, r.t. — 30 32
5 0.01 Grinding, r.t. — 20 37
6 0.03 Grinding, r.t. — 20 45
7 0.05 Grinding, r.t. — 20 91
8 0.07 Grinding, r.t. — 15 95
9 0.09 Grinding, r.t. — 15 90
10 0.1 Grinding, r.t. — 15 88
11 0.07 Reflux EtOH 4 h 55
12 0.07 Reflux EtOH/H2O (1 : 1) 3 h 60
13 0.07 Reflux H2O 7 h 20
14 0.07 Reflux Toluene 5 h 30
15 0.07 Reflux Chloroform 5 h 12
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a

Reaction conditions: benzaldehyde (1 mmol), dimedone (1 mmol), malononitrile (1 mmol), catalysts, under different conditions.

b

Isolated pure yield.

Fig. 10. Images depicting the progression of the reaction involving benzaldehyde, malononitrile, and dimedone can be observed for (a) the initial stage, (b) after 5 minutes, and (c) after 10 minutes.

Fig. 10

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We conducted a separate study to evaluate the effect of various catalysts such as Fe3O4, SiO2@Fe3O4, GPTMS@SiO2@Fe3O4 and mesalamine on the model reaction under optimized reaction conditions (Table 4). When the model reaction was tested in the presence of Fe3O4 and SiO2@Fe3O4 in EtOH under reflux conditions, product 4a was obtained in 50% and 40% yields, respectively (Table 4, entries 1 and 2).47 When the same reaction was carried out by GPTMS@SiO2@Fe3O4, no product was obtained (Table 4, entry 3). Similarly, when mesalamine alone was used under grinding conditions at room temperature, product 4a was formed in 68% yield (Table 4, entry 4). As can be seen, mesalamine/GPTMS@SiO2@Fe3O4 indicates superior catalytic activity compared to other catalysts (Table 4, entry 5).

Effects of various catalysts on the synthesis of 4aa.

graphic file with name d3ra06560j-u2.jpg
Entry Catalyst Conditions Yieldb (%)
1 Fe3O4 EtOH/reflux 50
2 SiO2@Fe3O4 EtOH/reflux 40
3 GPTMS@SiO2@Fe3O4 EtOH/reflux Trace
4 Mesalamine Grinding, r.t. 71c
5 Mesalamine/GPTMS@SiO2@Fe3O4 Grinding, r.t. 95
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a

Reaction conditions: benzaldehyde (1 mmol), dimedone (1 mmol), malononitrile (1 mmol), catalysts (0.07 g), under different conditions.

b

Isolated pure yield.

c

0.1 g catalyst was used.

With the optimized conditions in hand, the various aldehyde substrate scope, dimedone and malononitrile were applied as the model reaction and diverse aldehydes were examined for the annulation reaction of 4a–p (Table 5, entries 1–16). The obtained results indicated that the activity of the aromatic aldehydes like electron-withdrawing and electron-releasing properties could influence the annulation reaction of 4a–p. Aromatic aldehydes with functional groups like –NO2, –Br, –Cl, and –CN yielded the corresponding products in excellent yields and a short reaction time. Moreover, when aromatic aldehydes with functional groups like –Me, –N(Me)2, OMe, and –OH are used instead of electron-withdrawing groups, the corresponding products are obtained at lower yields.

Substrate scope for the 2-amino-4H-benzo[b]pyran derivativesa.

graphic file with name d3ra06560j-u3.jpg
Entry Products Time (min) Yieldb (%) Mp (°C)
Found reported
1 graphic file with name d3ra06560j-u4.jpg 15 95 229–231, 231–233 (ref. 47)
2 graphic file with name d3ra06560j-u5.jpg 12 89 212–214, 215–217 (ref. 47)
3 graphic file with name d3ra06560j-u6.jpg 12 91 216–217, 218–220 (ref. 47)
4 graphic file with name d3ra06560j-u7.jpg 7 96 223–225, 225–226 (ref. 47)
5 graphic file with name d3ra06560j-u8.jpg 7 95 178–180, 180–182 (ref. 47)
6 graphic file with name d3ra06560j-u9.jpg 30 90 221–223, 220–222 (ref. 47)
7 graphic file with name d3ra06560j-u10.jpg 35 89 201–203, 198–200 (ref. 47)
8 graphic file with name d3ra06560j-u11.jpg 12 88 192–194, 190–192 (ref. 47)
9 graphic file with name d3ra06560j-u12.jpg 30 90 221–223, 222–224 (ref. 47)
10 graphic file with name d3ra06560j-u13.jpg 35 93 180–182, 182–184 (ref. 47)
11 graphic file with name d3ra06560j-u14.jpg 15 92 152–154, 155–157 (ref. 47)
12 graphic file with name d3ra06560j-u15.jpg 20 89 212–214, 215–217 (ref. 47)
13 graphic file with name d3ra06560j-u16.jpg 15 92 216–218, 215–217 (ref. 47)
14 graphic file with name d3ra06560j-u17.jpg 7 91 223–225, 224–226 (ref. 47)
15 graphic file with name d3ra06560j-u18.jpg 20 89 178–179, 180–181 (ref. 47)
16 graphic file with name d3ra06560j-u19.jpg 20 90 246–248, 248–250 (ref. 47)
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a

Reaction conditions: various aldehydes (1 mmol), dimedone (1 mmol), malononitrile (1 mmol), catalysts (0.07 g) under the dry grinding method at room temperature.

b

Isolated pure yield.

Separation of the heterogeneous catalyst from the reaction medium is one of the main advantages of every catalytic process and also is highly desirable in medicinal and commercial applications. Hence, we tested the reusability of the nanocatalyst. The reusability of mesalamine/GPTMS@SiO2@Fe3O4 was evaluated in the reaction of 4-cyanobenzaldehyde, dimedone and malononitrile under optimized conditions (Fig. 11). From Fig. 11A, it can be seen that the nanocatalyst can be reused for 8 cycles with a slight loss in activity from 96% to 90% using an external magnet. Moreover, the nanocatalyst after being recovered eight times was investigated by TEM and FT-IR analyses, as depicted in Fig. 11B and C. Both TEM and FT-IR analyses confirmed that the nanocatalyst can be reused for 8 cycles without any change in the core–shell structure and functional groups.

Fig. 11. (A) Recycling of the nanocatalyst in 4d, (B) TEM image, and (C) FT-IR spectrum of the recovered nanocatalyst.

Fig. 11

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To demonstrate the ability of this procedure for synthesis on the gram scale, the scaled up synthesis of 4m was evaluated in the reaction of 3-nitrobenzaldehyde, dimedone and malononitrile under the dry grinding method at room temperature, and the results are summarized in Table 6 and Fig. 12. The reaction proceeded well and 4m was obtained in high yields. From Table 6, it can be seen that the reactions were carried out in various scales such as 5, 10, and 15 mmol and the products were 90, 88, and 85%, respectively.

Scaled up synthesis of 4m.

graphic file with name d3ra06560j-u20.jpg
Entry Scale (mmol) Isolated yield (%)
1 1 92
2 5 90
3 10 88
4 15 85
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Fig. 12. Images depicting the progression of the reaction involving 3-nitroaldehyde, malononitrile, and dimedone for gram scale synthesis (10 mmol). (a) The initial stage, (b) after 7 minutes, and (c) after 15 minutes.

Fig. 12

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A proposed reaction pathway is shown in Scheme 4. Initially, the mesalamine/GPTMS@SiO2@Fe3O4 led to the activation of the carbonyl group on the aldehyde and malononitrile, giving intermediates 1 and 2, respectively. In continuation, nucleophilic addition from intermediate 2 to intermediate 1 led to the generation of intermediate 3. This intermediate then loses molecular water by E1cB elimination to give intermediate arylidiene malononitrile 5. Next, in the presence of the catalyst, dimedone is transformed into its enolized form 4. This enolized form then proceeds to attack intermediate 5 by Michael addition, resulting in the formation of intermediate 6. Finally, the cyclization reaction of intermediate 6 and a hydrogen shift produced the 2-amino-4H-benzo[b]pyran derivatives 9.

Scheme 4. A possible pathway for mesalamine/GPTMS@SiO2@Fe3O4 catalyzed tandem Knoevenagel–Michael cyclocondensation.

Scheme 4

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This study and many selected processes reported in the literature are listed in Table 7 and compared with each other in terms of various parameters such as catalyst, reaction conditions, time and yield. For example, Mohammadzadeh50 and colleagues reported Ag/Fe3O4@starch as a nanocatalyst. The requirement for high temperature is a limitation of this method (Table 7, entry 7). Bhosale53 and co-workers disclosed an iodine catalyst. There are some serious problems with this method, including high loading of the catalyst, toxic catalyst, a low number of catalyst recycling cycles, tedious reaction conditions, and use of DMSO as solvent (Table 7, entry 10). Also, Kalantari52 and co-workers prepared a Fe3O4@NH2@TCT@HOProCu nanocatalyst. The main disadvantages of this method are prolonged reaction time and tedious procedure for catalyst synthesis (Table 7, entry 9). Table 7 clearly shows that our method is more efficient and effective in terms of conditions, yield, time and loading of catalyst than other previously reported methods.

Comparison of mesalamine/GPTMS@SiO2@Fe3O4 with selected processes reported in the literature for the tandem Knoevenagel–Michael cyclocondensation.

Entry Catalyst Reaction conditions Time (min or h)/yield (%)
1 CeCl3·7H2O (10 mol%) EtOH : H2O (4 : 2)/reflux 1–2.5 h/70–93%45
2 Fe3O4@GA@IG (20 mg) EtOH/reflux 15–110 min/78–92%46
3 EDA/(CH2)3@SiO2@Fe3O4 (0.05 g) Grinding/r.t. 10–25 min/89–97%47
4 NH4H2PO4/Al2O3 (0.03 g) EtOH/reflux 5–60 min/45–92%48
5 NiFe2O4@SiO2@H14[NaP5W30O110] (0.02 g) EtOH/ultrasonic/r.t. 5–15 min/81–94%49
6 NiFe2O4@SiO2@H14[NaP5W30O110] (0.02 g) EtOH/reflux 15–35 min/57–80%49
7 Ag/Fe3O4@starch (15 mg) EtOH/50 °C 8–17 min/84–95%50
8 Per-6-NH2–β-CD (0.09 mmol) Solvent-free/r.t. 1–7 min/67–97%51
9 Fe3O4@NH2@TCT@HOProCu (0.01 g) EtOH/reflux 24 h/75–97%52
10 Molecular iodine (10 mol%) DMSO, reflux, Δ 3.2–4 h/80–92%53
11 Mesalamine/GPTMS@SiO2@Fe3O4 Grinding/r.t. 7–35 min/88–96%
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Conclusions

In summary, we successfully designed and synthesized a novel mesalamine-functionalized magnetic nanoparticles (mesalamine/GPTMS@SiO2@Fe3O4) and fully characterized its structure using various physicochemical tools. The activity of this catalyst in the synthesis of 2-amino-3-cyano-4H-pyran derivatives of various aromatic aldehydes, dimedone and malononitrile under a dry grinding method at room temperature was studied. The as-synthesized nanocatalyst offers remarkable and attractive advantages including no need for solvent, environmental friendliness, economical processing, easy workup procedure, no need for column chromatography, multiple carbon–heteroatom and carbon–carbon bond formation, high product yield, and easy separation from the reaction environment. The as-synthesized nanocatalyst can be conveniently recovered from the reaction mixture by employing a magnetic bar, and then reused in the next run.

Conflicts of interest

There are no conflicts to declare.

Supplementary Material

RA-013-D3RA06560J-s001

Acknowledgments

The present study, derived from the MSc thesis by Mahdiyeh Partovi, was supported by the Iran National Science Foundation INSF and the University of Zanjan.

†

Electronic supplementary information (ESI) available: Copies of FT-IR, 1H NMR (250 MHz, CDCl3) and 13C NMR (62.5 MHz, CDCl3) spectra of the synthesized compounds. See DOI: https://doi.org/10.1039/d3ra06560j

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