A reaction mode of carbene-catalysed aryl aldehyde activation and induced phenol OH functionalization

Abstract

The research in the field of asymmetric carbene organic catalysis has primarily focused on the activation of carbon atoms in non-aromatic scaffolds. Here we report a reaction mode of carbene catalysis that allows for aromatic aldehyde activation and remote oxygen atom functionalization. The addition of a carbene catalyst to the aldehyde moiety of 2-hydroxyl aryl aldehyde eventually enables dearomatization and remote OH activation. The catalytic process generates a type of carbene-derived intermediate with an oxygen atom as the reactive centre. Inexpensive achiral urea co-catalyst works cooperatively with the carbene catalyst, leading to consistent enhancement of the reaction enantioselectivity. Given the wide presence of aromatic moieties and heteroatoms in natural products and synthetic functional molecules, we expect our reaction mode to significantly expand the power of carbene catalysis in asymmetric chemical synthesis.

Selective functionalization of aromatic compounds is important in synthetic chemistry. Here the authors report an N-heterocyclic carbene-catalysed approach for enantioselectively converting ortho-hydroxyaldehydes to cyclic products, via activation of both phenol and aldehyde groups.

Aromatic moieties are among the most common functional groups in natural products, bioactive molecules and polymeric materials. Thus, selective functionalization of aromatic molecules and their derivatives has received continuous attention in organic synthesis. Currently, the field of aromatic molecule functionalization, such as aromatic sp²-CH activation and benzylic sp³-CH activation, is dominated by transition metal catalysis¹,²,³. Organic catalyst-enabled activation of aromatic or benzylic carbon as reactive centre has been much less developed. Representative examples in this direction include photoredox/organocatalytic radical reactions from MacMillan and colleagues⁴ and Melchiorre and colleagues⁵, and amine-mediated reactions via an enamine or iminium intermediate from Melchiorre and colleagues⁶, Jørgensen and colleagues⁷, Chen and colleagues⁸ and Xu et al.⁹. In the area of N-heterocyclic carbene (abbreviated as NHC or carbene in this manuscript) organocatalysis¹⁰,¹¹, aldehydes¹²,¹³,¹⁴,¹⁵,¹⁶, esters¹⁷,¹⁸,¹⁹ and ketenes²⁰,²¹ have been widely employed as substrates. However, nearly all these reactions were focused on using carbon atoms in non-aromatic (and acyclic) molecules as the reactive sites (Fig. 1a). For example, the α and β-carbons of acyclic α,β-unsaturated aldehydes²² have been widely explored with a large set of asymmetric reactions. In contrast, aromatic aldehydes are only used in benzoin-type reactions. It remains challenging for the stereo-electronic power of the carbene catalyst to go across the conjugated bonds of the aromatic frameworks to induce activation and selective reactions (Fig. 1b). In 2013, we disclosed that the benzylic sp³-CH of indole-type heteroaryl aldehyde²³ could be activated via an analogous vinyl enolate intermediate (NHC-bound o-QDMs, Fig. 1b). However, the activation of simple aromatic aldehydes (such as benzaldehyde) without heteroatom incorporated in the aromatic rings remains difficult.

Figure 1. Activation modes in carbene organic catalysis.

(a) Previous studies mainly dealt with carbon atom activation for acyclic non-aromatic carbonyl compounds. (b) Our earlier studies realized indole-type heteroaryl aldehyde benzylic carbon activation. (c) Addition of carbene catalyst eventually leads to simple phenyl aldehyde activation which induces phenol oxygen atom functionalization via a new azolium-bound intermediate (II).

Here we demonstrate that the simple aryl aldehyde could be activated by a carbene catalyst (Fig. 1c). Addition of the carbene catalyst to the aldehyde moiety of 2-hydroxyl benzaldehyde (salicylaldehyde, 1a) eventually leads to acyl azolium intermediate I under an oxidative condition. The electron-withdrawing effect from the acyl azolium moiety, in combination with the electron-donating ability of the OH group, enables a dearomatization²⁴ process that forms azolium-bound ortho-quinone methide intermediate II (o-QM). Ortho-quinone methide is a reactive intermediate broadly used in the synthesis of sophisticated natural products and other functional molecules²⁵,²⁶. The oxygen atom in intermediate II behaves as an active site to react with ketone substrate 2a to afford chiral ketal-like 3a as the product. The overall process is a carbene-catalysed functionalization of the phenol OH group via a type of NHC-bound o-QMs intermediate (II). Notably, in nearly all of the reported reactions, only carbon atoms of the NHC-bound intermediates (Fig. 1a) were explored as the reactive centres²⁷,²⁸. The exceptions are NHC-mediated polymerization of lactone²⁹ and Breslow intermediate-induced ring expansion³⁰,³¹,³². Our present work realizes oxygen atom activation, in which the reactivity of the oxygen atom is modulated by the covalent-bound NHC catalyst in intermediate II. The azolium-bound ortho-quinone methides intermediate (II) constitutes a new mode for NHC catalysis. Additionally, we realize a urea/NHC cooperative catalytic process³³ (III, Fig. 1c), in which an achiral urea co-catalyst significantly and consistently improves the enantioselectivity of the reaction.

Results

Reaction optimizations

Key results of initial optimization of reaction conditions are summarized in Table 1. Salicylaldehyde (1a) and trifluoroacetophenone (2a) were chosen as the model substrates to form 1,3-dioxin-4-one (3a). Studies on the solvent effects (see Supplementary Tables 2 and 3) found that a mixture of CH₂Cl₂/hexane (1:1, v/v) is the optimal choice. Quinone (DQ), first explored by Studer and colleagues in NHC catalysis³⁴, is an effective oxidant. Several bases (see Supplementary Table 1) could produce the desired product in such transformations. In the absence of NHC catalyst, product 3a was not formed. The two starting materials (1a and 2a) remained unreacted and could be recovered (entry 1). The search for NHC catalysts found that aminoindanol-derived triazolium precatalyst C1 with an N-mesityl substituent (first explored by Bode³⁵) could mediate the formation of 3a in 58% yield and with 63:37 e.r. (entry 2). The reaction yield could be dramatically increased to 97% when precatalyst C2 with an N-trichlorophenyl substituent (first explored by Rovis³⁶) was used (entry 3). Decreasing the reaction temperature from room temperature to −10 °C led to a small but consistent improvement in the e.r. value without affecting the reaction yield (entry 4). Further decreasing the reaction temperature, however, slowed down the reaction without enhancing the enantioselectivity. We then turned to identifying conditions that could improve the reaction enantioselectivity. In our studies on the solvent effects (see Supplementary Table 2), we found that solvents could affect the reaction enantioselectivity. For example, when THF was used as the solvent, the e.r. value of 3a decreased from 73:27 to 52:48 (entry 4 versus 5). These results suggest that non-covalent interaction is likely to play an important role in controlling the enantioselectivity of our reactions. We thus examined non-covalent organic catalysts and found that using achiral thiourea³⁷,³⁸,³⁹,⁴⁰,⁴¹ A1 as a co-catalyst could improve the e.r. values of 3a from 73:27 to 85:15 (entry 6 versus 4). Increasing the amount of A1 led to a lower yield of 3a with little benefit to the enantioselectivity (entry 7). Further studies found that both thiourea and urea⁴² co-catalysts can improve the enantioselectivity (entries 8 and 9, and see Supplementary Table 4). We finally found that using asymmetric urea A3 could lead to 3a in 99% yield and with 94:6 e.r. (entry 9). The loading of the NHC catalyst (C2) could be decreased to 5 mol%, without affecting the reaction yield and e.r. (entry 11). The urea co-catalyst likely forms hydrogen-bonding interactions with the ketone substrate (for example, 2a) and/or intermediate II (Fig. 1c) to improve the reaction enantioselectivity. The hydrogen-bonding interactions are sensitive to solvents. For example, switching the solvent from CH₂Cl₂/hexane to THF led to a dramatic drop in enantioselectivity (entries 10 versus 11).

Table 1. Reaction of salicylic aldehyde with ketone.

Substrate scope with 2-hydroxyl aryl aldehydes

With an acceptable reaction condition in hand (Table 1, entry 11), the generality of the reaction was then explored. First, we studied the scope of the 2-hydroxyl aryl aldehydes (Table 2). With trifluoroacetophenone 2a as a model electrophile, different substituents and substitution patterns on the phenyl ring were examined. Electron-releasing substituents such as alkyl (3b, 3d and 3k) and alkoxyl (3c, 3g and 3j) units on the phenyl ring of the aldehyde substrates were well tolerated. Electron-withdrawing groups such as halogen atoms (3e, 3f and 3h) and carboxylic ester units (3i) could also be placed on the phenyl ring of the aldehyde substrates. It is worth noting that the steric effect of substituents in different positions on the phenyl ring does not affect the results, as seen for the substrates with 3- and 6- substituents on the 2-hydroxyl aryl aldehydes, but these substitution patterns both led to very good yields and e.r. (3j, 3k and 3l). Product 3m bearing a sesamol moiety (3,4-methylenedioxyphenol) could also be made by our method. The benzene ring of 1a could be extended to other aromatic frameworks, such as naphthyl units (3n–3p). Additionally, steric influence has little effect on the reaction outcomes for all the three naphthaldehyde substrates (3n–3p). Notably, in all cases, the reactions were highly efficient, and the products were obtained in excellent yields. The two starting materials were used with nearly a 1:1 ratio.

Table 2. Examples of 2-hydroxyl aryl aldehyde substrates.

Substrate scope with trifluoromethyl ketones

We next examined the reactions of trifluoromethyl ketone substrates 2 in our standard condition (Table 3). Here we chose 5-methylsalicyladehyde (1b) as a model aldehyde substrate because it is easier to handle than 1a, as 1b is a solid at room temperature and stable toward air-oxidation. Different substituents and substitution patterns on the phenyl ring of the ketone substrates were all tolerated (3b and 3q–3x). Electron-donating groups such as methyl (3q), methoxy (3r) and N,N-dimethyl amino (3s) groups on the phenyl para-position were all tolerated, giving the corresponding products with excellent values of yield and e.r. Electron-withdrawing substituents on the phenyl meta- or para- position (3t, 3x) had little effect on the yields and selectivities. The phenyl substituent of ketone 2a could be replaced by a heteroaryl substituent (3y). Alkyl substituted trifluoromethyl ketones are typically challenging substrates when used as electrophiles because of the ketone/enol isomerization. These substrates could be used in our reactions as well (3z, 3za), albeit with a small to moderate drop in the yield and e.r. values.

Table 3. Scope of trifluoromethyl ketones.

DFT studies on NHC-bound intermediate II

DFT calculations were used to assess the nature of o-QM in intermediate II. The computational details are provided in the Supplementary Figs 56–65. Six conformers of II were obtained from DFT calculations. The optimized structure of the most stable conformer of intermediate II (II-1), which can later react with ketone 2a, is shown in Fig. 2a. Other less stable structures are shown in the Supplementary Information. We also calculated Mulliken atomic charges for II-1 and found that the O1 and O2 atoms have partial negative charges of −0.33 and −0.47, respectively (Fig. 2b); the magnitudes of these values are significantly smaller than 1. These fractional charges imply that II-1 cannot be described as either of the two extreme resonance structures depicted in Fig. 2b; instead, the real state of o-QM should lie somewhere in between.

Figure 2. DFT studies of intermediate II and the roles of urea co-catalyst.

(a) Structure of II and key interatomic distances (in Å). (b) Resonance structures of II. (c) Schematic drawing of A3-TS2_1-A. (d) NCI plot for A3-TS2_1-A. Green surfaces represent attractive interactions. Some atoms are omitted for clarity. (e) NCI plots for A3-TS2_1-A and A3-TS2_1-A-minor. Relative free energies (kcal mol⁻¹) are with respect to A3-TS2_1-A.

DFT studies on the mechanisms of [4+2] annulation

To gain mechanistic insights, DFT calculations were performed for the reaction between intermediate II and ketone substrate 2a in the presence or absence of a urea co-catalyst, taking into account the solvent effect of DCM (see the Supplementary Tables 6–11 for details). The calculations without urea suggest that NHC-bound intermediate II can react with 2a in a [4+2] mechanism (Fig. 1c) to afford a ketal-like product, without having very high barriers, thus supporting the hypothesis regarding the involvement of o-QM in the reaction. The four conformers (II-1, II-2, II-3 and II-4) of intermediate II in Supplementary Fig. 59 can react with 2a, giving rise to several possible reaction pathways (16 pathways in total). DFT calculations without urea showed that this reaction consists of two steps: (1) a ring-annulation step and (2) an NHC dissociation step, and that step 2 should be the rate-determining step (see the Supplementary Information). On the basis of this result, we performed further calculations with co-catalyst A3.

The lowest-energy transition state for the rate-determining step on Path 1-A (A3-TS2_1-A) with urea A3 is connected to the major product. In this transition state, unlike our initial guess (Fig. 1c), urea A3 forms hydrogen bonds preferentially with the carbonyl oxygen atom of the o-QM moiety (Fig. 2c), rather than with the trifluoromethyl ketone substrate (Fig. 1c). A3-TS2_1-A has attractive π-π stacking between the pentafluorophenyl group of A3 and the indane moiety of the catalyst (Fig. 2d). Such π-π stacking is also observed in A3-TS2_1-A-minor, but not in the other A3-TS2's. The somewhat greater stability of A3-TS2_1-A compared with A3-TS2_1-A-minor is attributed to the attractive dispersion interactions between the urea moiety and the phenyl group from ketone (Fig. 2e), which are prominent only in A3-TS2_1-A. Our calculations therefore highlight the importance of dispersion interactions in determining the enantioselectivity.

Application of the [4+2] annulation products

Our reaction is amenable for large-scale synthesis (Fig. 3a). Notably, in the gram scale synthesis, the use of 1 mol% NHC precatalyst was sufficient to produce 3b (1.5 g) in 98% yield and with 96:4 e.r. Additionally, the organic oxidant (DQ) could be used in catalytic amount by using inexpensive MnO₂ as a terminal oxidant⁴³ (Fig. 3b).

Figure 3. Scalable and practical synthesis.

(a) Gram scale synthesis with 1 mol% NHC loading. (b) Reaction using MnO₂ as terminal oxidant.

The products of our catalytic reactions contain a benzo[1,3]dioxin scaffold. This chiral benzo[1,3]dioxin unit itself and its closely related structures are widely found in natural products and bioactive synthetic molecules. Examples of such molecules include natural product Epicocconigrone A with anticancer activities⁴⁴ and Efavirenz, commercially used as an HIV reverse transcriptase inhibitor⁴⁵. Our laboratories are interested in the antiviral and antibacterial activities of these compounds for agricultural use⁴⁶,⁴⁷,⁴⁸. Therefore, we then evaluated the in vitro bioactivities of our products against several types of bacteria and fungi that can cause plant infections (Table 4). The commercially available and commonly applied bactericide Kresoxim-methyl was used as the positive control, and dimethyl sulfoxide was used as the negative control. Preliminary studies found that several of our compounds showed significant activities against Eggplant Verticillium, Phytophthora infestans and Fusarium oxysporum. For example, compound 3l showed 25–38% inhibition rates against the above three fungi at a concentration of 50 μg ml⁻¹.

Table 4. The antifungal activity of our products.

	Inhibition rate (%)
Sample	Eggplant Verticillium	Phytophthora infestans	Fusarium oxysporum
3c	26.10±0.64	26.47±2.45	26.71±2.18
3b	34.98±2.92	16.98±6.26	11.50±2.75
3i	3.60±1.61	10.49±0.93	4.71±1.06
3l	32.91±1.36	38.58±0.59	25.65±0.61
Positive control	100	84.00±3.59	69.61±2.54
Negative control	0	0	0

Inhibitory effects of compounds at a concentration of 50 μg ml⁻¹. Each data is the average of three replicates. Kresoxim-methyl was used as the positive control, Dimethyl sulfoxide was used as negative control.

Discussion

In short, we have developed a reaction mode of carbene-catalysed activation of aryl aldehydes. Addition of the carbene catalyst to the aldehyde moiety eventually leads to remote phenol OH activation and dearomatization. The catalytic reaction involves an NHC-bound intermediate (o-QMs) with the oxygen atom acting as the reactive centre. A hydrogen-bond donating co-catalyst (urea or thiourea) works cooperatively with the NHC catalyst, resulting in significant and consistent enhancement of the reaction enantioselectivity. Our method is amenable for large-scale enantioselective synthesis with relatively low loading of the NHC catalyst. Preliminary studies on the bioactivities of our compounds identified a few leads with antifungal activities. We expect our study to encourage further exploration on new reaction modes and alternative intermediates with NHC organic catalysis. Our findings of NHC/urea cooperative catalysis will provide some possibilities in controlling challenging stereoselectivities, for example, in remote group functionalizations.

Methods

General strategy of [4+2] annulations

To a 10 ml flame-dry Schlenk reaction tube equipped with a magnetic stir bar, chiral NHC pre-catalyst C2 (0.005 mmol, 5 mol%, 2.4 mg), urea A3 (0.02 mmol, 20 mol%, 8.76 mg), DABCO (0.1 mmol, 100 mol%, 11.2 mg), oxidant DQ (0.11 mmol, 110 mol%, 45 mg), aldehyde (0.11 mmol) and 4 Å molecular sieves were added. The Schlenk tube was sealed with a septum, evacuated and refilled with nitrogen (3 cycles). Solvent (CH₂Cl₂/hexane=1:1, 2.0 ml) and trifluoromethyl ketone 2 (0.1 mmol) were then added via syringe. The reaction mixture was allowed to stir for 24 h at −10 °C. After completion of the reaction, monitored by a TLC plate, the reaction mixture was concentrated under reduced pressure, and the residue was subjected to column chromatography or TLC plate directly using hexane/EtOAc as eluent to afford the desired product 3. For ¹H, ¹³C, ¹⁹F NMR and high-performance liquid chromatography spectra of compounds in this manuscript, see Supplementary Figs 1–54.

Data availability

The X-ray crystallographic coordinates for structures reported in this article have been deposited at the Cambridge Crystallographic Data Centre (3h: CCDC 1486140). These data could be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif. For XYZ coordinates of optimized structures in DFT studies on the mechanism, see Supplementary Data 1.

Additional information

How to cite this article: Chen, X. et al. A reaction mode of carbene-catalysed aryl aldehyde activation and induced phenol OH functionalization. Nat. Commun. 8, 15598 doi: 10.1038/ncomms15598 (2017).

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Supplementary Material

Supplementary Information

Supplementary figures, supplementary tables, supplementary methods and supplementary references.

Supplementary data 1

In DFT study, XYZ coordinates of optimized structures are important parameters to understand the calculation models. For XYZ coordinates of optimized structures in DFT studies on the mechanism, see Supplementary Data 1.