Molecular Iodine-Catalyzed Selective C-3 Benzylation of Indoles with Benzylic Alcohols: A Greener Approach toward Benzylated Indoles

Abstract

Iodine-catalyzed selective C-3 benzylation of indoles with benzylic alcohols is developed. The reaction proceeds with molecular iodine as the catalyst under ligand-, metal-, and base-free conditions and tolerates wide functionalities. The experimental observations account for the halogen-bond activation mechanistic pathway for the molecular iodine catalysis.

Introduction

Heterocyclic compounds are the core building units for the design and synthesis of new molecular entities for drug discovery. Among the myriad of bioactive molecules, a large number of molecules encompass indole derivatives.¹ Substituted indoles are of immense interest as they found applications as pharmaceuticals, drugs, agrochemicals, and in materials science.² Most of the biologically relevant indole alkaloids are C-3-substituted, for example, natural amino acid tryptophan and the neurotransmitter serotonin.³

Traditionally, C-3 benzylation of indoles was achieved mainly via Friedel–Crafts reactions or S_N² reaction of benzyl halides with indoles.⁴ However, the use of a stoichiometric amount of Lewis acids and formation of unwanted by-products reduce the effectiveness of these methodologies.⁵ Therefore, the demand for mild, efficient, and economic methods for the direct alkylation of indoles remains an area of active research.⁶

Benzylic alcohols are gaining interest as green alkylating agents as the only by-product generated is water, thereby producing an environmentally benign and clean process⁷ compared to the use of corresponding halides, esters, carboxylates, or related compounds for this purpose.⁸

In the past few years, many studies have reported the C-3 benzylation reactions by using expensive transition metal complex based catalytic systems with Fe,⁹ Ir,¹⁰ Au,⁷ In,⁸ Pd,¹¹ Pt,¹² and Ru,¹³ which are moisture- and air-sensitive,^8,9 and their preparation process needed complex handling^10,12 and harsh conditions,^8,10,12 which limit their practical utility in a large scale. Some methods required the addition of oxidants, ligands,^7,10 bases,^9,10 or other additives¹³ to maximize the catalyst activity and complete their catalytic pathway. Metal-free processes are always favorable in the pharmaceutical industry due to the additional difficulties associated with the metal impurities.¹⁴

Therefore, there is rising demand for the development of metal-free catalytic systems for C-3 benzylation, which has been less explored to date and will be a beneficial alternative to transition-metal catalysis. Yus and co-workers have reported noncatalytic C-3 alkylation by alcohols through a hydrogen-autotransfer strategy with a stoichiometric amount of base.¹⁵ There are reports of C-3 benzylation catalyzed by Br_2,¹⁶ N-heterocyclic carbene,¹⁷ high-temperature water,¹⁸ and some Lewis¹⁹ and Brønsted acids.²⁰ In recent times, molecular iodine has emerged as a green and environmentally benign reagent and has been successfully employed as a catalyst in different organic transformations forming new C–C, C–N, C–O, and C–S bonds in organic compounds.²¹ It is naturally abundant, inexpensive, nontoxic, environmentally friendly, and active even in very small amounts.²² Inspired by its catalytic activeness and economic viability,²³ we herein report a green, efficient, and economical strategy for C-3 selective benzylation of indoles employing molecular iodine as a catalyst under ligand-, metal-, and base-free conditions (Scheme 1).

Scheme 1. C-3 Benzylation of 1-Methylindole (1a).

Results and Discussion

The studies were initiated with 1-methylindole and diphenylmethanol as substrates to establish the best reaction conditions. It was found that 1-methylindole and diphenylmethanol when treated with molecular iodine (5 mol %) in toluene at 40 °C produced the C-3 benzylated product in 85% yield in 5 h (Table 1, entry 1).

Table 1. Screening of the Effect of Catalysts and Solvents^a.

entry	catalyst	solvent	time (h)	yield (%)
1	I2	toluene	5	85
2		toluene	12	nr
3b	I2	toluene	7	83
4c	I2	toluene	7	70
5d	I2	toluene	7	85
6e	I2	toluene	7	65
7f	I2	toluene	7	85
8	KI	toluene	12	nr
9	I2	DCM	7	67
10	I2	MeCN	7	72
11	I2	1,4-dioxane	7	78
12	I2	DMSO	10	nr
13	I2	DMF	10	nr
14	I2	H2O	7	nr
15	I2	MeOH	7	nr
16	I2	EtOH	7	nr

^aReaction conditions: 1a (1.2 equiv), 2a (1 equiv), catalyst (5 mol %), solvent (2 mL), temp (40 °C), time (5 h), in air.

^bTemp (60 °C).

^cCatalyst (2 mol %).

^dCatalyst (10 mol %).

^eRoom temperature.

^fN₂ atmosphere.

C-3-substituted product formation is confirmed by the presence of characteristic peaks at δ 118.3 (for C-3) and 127.4 (for C-2) in ¹³C{¹H} NMR (100 MHz, CDCl₃).⁷ The single-crystal structure of 3a further confirms the C-3 selectivity of the reaction. The crystal structure is solved and refined in the orthorhombic space group Pna21, with one symmetry independent molecule in the lattice ORTEP with 50% probability ellipsoids displayed in Figure 1. Details of the single-crystal X-ray data collection method, crystal data parameter table, CIF, and Check CIF report are available in the Supporting Information.

Figure 1.

Single-crystal structure of 3a.

No desired product was observed in the absence of the I₂ catalyst even after 12 h (Table 1, entry 2). Hence in order to study the activity of iodine as a catalyst, reactions were performed by varying the amount of catalyst. Use of 2 mol % catalyst gave lower yield (Table 1, entry 4), and an increased amount of 10 mol % catalyst gave no significant improvement in the yield (Table 1, entry 5). The highest activity was observed using 5 mol % catalyst (Table 1, entry 1). In order to study the effect of temperature, the reactions were performed by varying the conditions at rt, 40 °C, and 60 °C, and the best result was observed at 40 °C (Table 1, entries 1, 3, and 6). Performing under a N₂ atmosphere produced similar results indicating no role of oxygen in the reaction (Table 1, entry 7). The effects of other iodine-containing additives were investigated at 40 °C, and no reaction was observed with 5 mol % KI (Table 1, entry 8), which proved the effectiveness of I₂ as a catalyst for the current protocol. Most of the aprotic solvents such as toluene, DCM, MeCN, and 1,4-dioxane resulted in acceptable yields (Table 1, entries 1, and 9–11) except for DMSO and DMF where no product formation was observed even after extended reaction times (Table 1, entries 12 and 13). In contrast, no reaction proceeded at all in protic solvents such as H₂O, MeOH, and EtOH (Table 1, entries 14–16). From the study of the influence of the solvent on the reaction, some important conclusions on the mode of iodine catalysis can be drawn. In the presence of protic solvents, iodine is known to decompose slowly to form Brønsted acid HI, which is responsible for further reaction catalysis.²¹ However, from the observations of Table 1, no reaction proceeded at all in protic solvents such as H₂O, MeOH, and EtOH (Table 1, entries 14–16), which clearly rules out the contribution of Brønsted acid mode of catalysis by molecular iodine. On the other hand, iodine in most aprotic solvents gave acceptable yields (Table 1, entries 1 and 9–11), which accounts for the halogen-bond activation mechanism of molecular iodine.²¹ It also explains why no product formation was observed in DMSO and DMF despite being aprotic solvents as they are expected to form strong halogen bonds with molecular iodine resulting in deactivation of the catalyst for further reaction.²¹ The reaction did not require any external base or additives.

The scope and limitations of the C-3 benzylation of indoles were investigated based on electronically diverse indole and benzyl alcohol derivatives. The results are summarized in Scheme 2. Benzyl alcohols with both electron-donating substituents such as Me and OMe (Scheme 2: 3e, 3h–3k) and electron-withdrawing substituents such as Cl and Br (Scheme 2: 3c, 3d, 3f, 3q) afforded products in good yields (70–92%). Primary benzylic alcohols with electron-donating substituents (OMe) resulted in the desired product in 83% yield (Scheme 2: 3j), whereas electron-poor or unsubstituted primary benzylic alcohols resulted in no reaction. This observation can be explained by the increased stability of intermediate species formed during the process in the presence of electron-rich benzylic systems. In contrast, secondary benzylic alcohols bearing both electron-donating and electron-withdrawing groups afforded the benzylated products in 80–90% yield (Scheme 2: 3a–3i, 3k). Tertiary benzylic alcohols showed highest reactivity and resulted in the desired products in 90–92% yield (Scheme 2: 3l, 3m), which can be attributed to the carbocation stability. Interestingly, if the 3-position of indole is preoccupied, the reaction proceeds at the 2-position (Scheme 2: 3n). Sensitive functionalities such as Br, Cl, carbonyl, and OMe remained unaffected under the reaction conditions. The protocol was also examined for chain alkyl alcohol but produced no significant result.

Scheme 2. C-3 Benzylation of Indole with Benzyl Alcohols.

Reaction conditions: indole (1.2 equiv), alcohol (1 equiv), iodine (5 mol %), toluene (2 mL), temp (40 °C), time (5 h), in air.

From Table 1, it was observed that no reaction proceeds in protic solvents due to the decomposition of iodine into HI ruling out Brønsted acid mode of catalysis. To experimentally prove the contribution of the halogen-bond activation mechanism of molecular iodine in our catalytic pathway, the following experiments were performed. 1-Methylindole and diphenylmethanol when treated with molecular iodine in toluene at 40 °C produced the C-3 benzylated product in 85% yield in 5 h (Table 2, entry 1). On the other hand, addition of aqueous HI (57 wt %) produced only 26% of the desired product, which supported our earlier observation on solvent effects and excluded the contribution of Brønsted acid mode of catalysis for the reaction pathway (Table 2, entry 5). We analyzed the influence of trace amounts of water (the amount of water present in aqueous HI) in the reaction on the catalytic activity of molecular iodine and observed no comparable change in reactivity (Table 2, entry 2). The catalytic activity of molecular iodine is suppressed by the addition of KI due to the formation of triiodide ions,²⁴ which is evident from the lowered reaction yield (Table 2, entry 3) whereas the activity of HI remains unchanged (Table 2, entry 6). Addition of a molecular sieve (25 mg) resulted in no change in reactivity of molecular iodine (Table 2, entry 4) indicating no moisture sensitivity.

Table 2. Comparative Study of I₂ and HI Mode of Catalysis^a.

entry	catalyst	yield (%)b
1	I2	85
2	I2 + H2Ob	82
3	I2 + KI	43
4	I2 + MS	86
5	HI	26
6	HI + KIc	26

^aReaction conditions: 1-methylindole (1.2 equiv), diphenylmethanol (1 equiv), catalyst (5 mol %), solvent (2 mL), temperature (40 °C), time (5 h), in air.

^b28 mol % water.

^c1 equiv of KI.

From the experimental observations and literature findings, a plausible mechanism has been proposed as shown in Scheme 3. The first step is expected to be the activation of alcohol by iodine forming a halogen bond between the oxygen of benzyl alcohol 1 and molecular iodine.^21a The oxygen atom of the alcohol bears a partial positive charge due to the halogen bonding and forms an intermediate species as shown in 2, which is stabilized by the resonance effect (+R effect) of the phenyl rings attached to the nearby secondary carbon center. In the presence of strong π-nucleophile indole 3, an electrophilic substitution reaction takes place at the C-3 position of the indole ring (the most nucleophilic center on the indole nucleus) to form an intermediate species 4, which undergoes rearomatization to form 3-benzylated indole 5 with elimination of water and regeneration of molecular iodine to complete the catalytic cycle. No generation of any other side products in the reaction was observed. The stability of the intermediate species 2 can be increased by introducing electron-donating substituents to the phenyl rings or using tertiary benzyl alcohols.

Scheme 3. Plausible Mechanism.

Conclusions

In summary, we have developed a protocol for the C-3 selective benzylation of indoles with benzylic alcohols employing molecular iodine as a green catalyst. Our protocol is simple and environmentally benign and proceeds under ligand-, metal-, and base-free conditions. The mild conditions and wide functional group tolerance make the protocol suitable for further applications.

Experimental Section

General Information

All reactions were carried out using Tarsons Spinot digital magnetic stirrers under standard conditions. Analytical thin layer chromatography (TLC) was carried out on Merck silica gel 60F254 plates using short wave (254 nm) UV light. Column chromatography purifications were performed over silica gel (100–200 mesh). ¹H and ¹³C{¹H} NMR spectra were recorded on a JEOL JNM ECS NMR spectrometer (400 and 100 MHz, respectively) using CDCl₃ as the solvent and TMS as the internal standard. Chemical shifts (δ) are reported in parts per million (ppm) relative to the central peak of the solvent. Multiplicities are indicated as s (singlet), d (doublet), t (triplet), q (quartet), m (multiplet), dd (doublet of doublet), and br (broad). Coupling constants (J values) are given in hertz (Hz). HRMS data were recorded via electrospray ionization with a Q-TOF mass analyzer. Single-crystal X-ray diffraction spectra were collected on a Bruker SMART APEX-II CCD diffractometer using Mo Kα (λ =0.71073 Å) radiation. Melting points were recorded in a digital melting point apparatus and are uncorrected. All chemicals used were purchased commercially and used without further purification. Solvents used for extraction and chromatographic separations were distilled prior use.

General Procedure for C-3 Benzylation of Indoles with Benzylic Alcohols

A round-bottom flask was charged with indole 1 (1 mmol) and alcohol 2 (0.8 mmol) in the presence of 5 mol % (0.05 mmol, 12.6 mg) molecular iodine (I₂) in toluene (2 mL) at 40 °C for 5 h. After completion of reaction (confirmed by TLC), the reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was dried over Na₂SO₄ and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel, hexane/ethyl acetate) to give the desired products 3a–3s.

3-Benzhydryl-1-methyl-1H-indole (3a)

Following the general procedure, 3a was obtained as a white solid, 252 mg, 85% yield; mp 142–144 °C; ¹H NMR (400 MHz, CDCl₃): δ 7.26–7.18 (m, 13H), 6.97–6.92 (m, 1H), 6.35 (s, 1H), 5.64 (s, 1H), 3.64 (s, 3H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 144.1, 137.4, 129.0, 128.7, 128.2, 127.4, 126.1, 121.6, 120.0, 118.8, 118.3, 109.1, 48.8, 32.6.

3-Benzhydryl-1H-indole (3b)

Following the general procedure, 3b was obtained as a white solid, 246 mg, 87% yield; mp 121–123 °C; ¹H NMR (400 MHz, CDCl₃): δ 7.94 (s, 1H), 7.35 (d, J = 8.2 Hz, 1H), 7.30–7.14 (m, 12H), 6.98 (t, J = 7.3 Hz, 1H), 6.57 (s, 1H), 5.67 (s, 1H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 143.9, 136.7, 135.7, 129.0, 128.3, 127.0, 126.2, 124.0, 122.1, 119.9, 119.4, 111.0, 48.8.

3-[(4-Chlorophenyl)(phenyl)methyl]-1-methyl-1H-indole (3c)

Following the general procedure, 3c was obtained as a colorless liquid, 292 mg, 88% yield; ¹H NMR (400 MHz, CDCl₃): δ 7.30–7.14 (m, 12H), 6.98 (t, J = 7.3 Hz, 1H), 6.38 (s, 1H), 5.63 (s, 1H), 3.69 (s, 3H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 143.6, 142.6, 137.4, 131.9, 130.3, 128.9, 128.7, 128.4, 127.1, 126.4, 121.8, 119.8, 118.9, 117.7, 109.2, 48.1, 32.7.

3-[(4-Bromophenyl)(phenyl)methyl]-1-methyl-1H-indole (3d)

Following the general procedure, 3d was obtained as a colorless liquid, 312 mg, 83% yield; ¹H NMR (400 MHz, CDCl₃): δ 7.38 (d, J = 8.7 Hz, 2H), 7.27–7.25 (m, 3H), 7.20–7.17 (m, 5H), 7.09 (d, J = 8.2 Hz, 2H), 6.97 (t, J = 8.2 Hz, 1H), 6.38 (s, 1H), 5.60 (s, 1H), 3.67 (s, 3H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 143.5, 143.2, 137.5, 131.3, 130.7, 128.9, 128.7, 128.4, 127.2, 126.4, 121.8, 120.0, 119.8, 118.9, 117.7, 109.2, 48.2, 32.6.

1-Methyl-3-[phenyl(p-tolyl)methyl]-1H-indole (3e)

Following the general procedure, 3e was obtained as a colorless liquid, 280 mg, 90% yield; ¹H NMR (400 MHz, CDCl₃): δ 7.27–7.15 (m, 8H), 7.09 (q, J = 8.2 Hz, 4H), 6.96 (t, J = 7.8 Hz, 1H), 6.39 (s, 1H), 5.63 (s, 1H), 3.68 (s, 3H), 2.32 (s, 3H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 144.4, 141.1, 137.5, 135.6, 129.0, 128.9, 128.7, 128.2, 127.4, 126.1, 121.6, 120.0, 118.8, 118.5, 109.1, 48.4, 32.6, 21.0.

3-[(4-Chlorophenyl)(phenyl)methyl]-1H-indole (3f)

Following the general procedure, 3f was obtained as a colorless liquid, 276 mg, 87% yield; ¹H NMR (400 MHz, CDCl₃): δ 7.96 (br s, 1H), 7.34 (d, J = 8.2 Hz, 1H), 7.29–7.13 (m, 11H), 6.98 (t, J = 7.8 Hz, 1H), 6.54 (s, 1H), 5.62 (s, 1H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 143.4, 142.4, 136.7, 132.0, 130.3, 128.9, 128.4, 126.8, 126.4, 124.0, 122.2, 119.8, 119.5, 119.4, 111.1, 48.2.

1-Methyl-3-(1-phenylethyl)-1H-indole (3g)

Following the general procedure, 3g was obtained as a colorless liquid, 183 mg, 78% yield; ¹H NMR (400 MHz, CDCl₃): δ 7.36 (d, J = 7.8 Hz, 1H), 7.30–7.24 (m, 5H), 7.21–7.14 (m, 2H), 6.99 (t, J = 7.8 Hz, 1H), 6.82 (s, 1H), 4.36 (q, J = 6.9 Hz, 1H), 3.73 (s, 3H), 1.69 (d, J = 7.3 Hz, 3H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 146.9, 137.3, 128.3, 127.4, 127.2, 125.9, 125.8, 121.5, 120.0, 119.7, 118.6, 109.1, 36.9, 32.6, 22.5.

1-Methyl-3-[1-(p-tolyl)ethyl]-1H-indole (3h)

Following the general procedure, 3h was obtained as a colorless liquid, 206 mg, 83% yield; ¹H NMR (400 MHz, CDCl₃): δ 7.38 (d, J = 7.8 Hz, 1H), 7.25 (t, J = 8.2 Hz, 1H), 7.17 (t, J = 7.8 Hz, 3H), 7.07 (d, J = 7.8 Hz, 2H), 6.99 (t, J = 7.3 Hz, 1H), 6.82 (s, 1H), 4.33 (q, J = 6.9 Hz, 1H), 3.73 (s, 3H), 2.30 (s, 3H), 1.67 (d, J = 6.9 Hz, 3H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 143.9, 137.3, 135.2, 129.0, 127.3, 127.2, 125.8, 121.4, 120.1, 119.7, 118.5, 109.0, 36.4, 32.6, 22.6, 21.0.

3-[1-(4-Methoxyphenyl)ethyl]-1-methyl-1H-indole (3i)

Following the general procedure, 3i was obtained as a colorless liquid, 233 mg, 88% yield; ¹H NMR (400 MHz, CDCl₃): δ 7.36 (d, J = 8.2 Hz, 1H), 7.26–7.14 (m, 4H), 6.99 (t, J = 7.3 Hz, 1H), 6.82–6.79 (m, 3H), 4.32 (q, J = 6.9 Hz, 1H), 3.76 (s, 3H), 3.73 (s, 3H), 1.66 (d, J = 7.3 Hz, 3H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 157.7, 139.1, 137.3, 128.3, 127.2, 125.8, 121.4, 120.3, 119.8, 118.5, 113.6, 109.0, 55.2, 36.0, 32.6, 22.6.

3-(4-Methoxybenzyl)-1-methyl-1H-indole (3j)

Following the general procedure, 3j was obtained as a colorless liquid, 208 mg, 83% yield; ¹H NMR (400 MHz, CDCl₃): δ 7.51 (d, J = 7.8 Hz, 1H), 7.27 (d, J = 8.2 Hz, 1H), 7.23–7.18 (m, 3H), 7.06 (t, J = 7.3 Hz, 1H), 6.82 (d, J = 8.2 Hz, 2H), 6.72 (s, 1H), 4.04 (s, 2H), 3.78 (s, 3H), 3.71 (s, 3H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 157.7, 137.1, 133.5, 129.5, 127.8, 127.0, 121.5, 119.2, 118.7, 114.7, 113.7, 109.1, 55.2, 32.5, 30.6.

3-[1-(p-Tolyl)ethyl]-1H-indole (3k)

Following the general procedure, 3k was obtained as a colorless liquid, 193 mg, 82% yield; ¹H NMR (400 MHz, CDCl₃): δ 7.88 (br s, 1H), 7.37 (d, J = 7.8 Hz, 1H), 7.31 (d, J = 8.2 Hz, 1H), 7.18–7.15 (m, 2H), 7.12 (d, J = 7.3 Hz, 1H), 7.07 (d, J = 7.8 Hz, 2H), 6.99 (t, J = 7.3 Hz, 2H), 4.33 (q, J = 7.3 Hz, 1H), 2.29 (s, 3H), 1.68 (d, J = 7.3 Hz, 3H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 143.8, 136.6, 135.3, 129.0, 127.3, 126.9, 121.9, 121.7, 121.0, 119.7, 119.1, 111.0, 36.5, 22.5, 21.0.

1-Methyl-3-(2-phenylpropan-2-yl)-1H-indole (3l)

Following the general procedure, 3l was obtained as a colorless liquid, 229 mg, 92% yield; ¹H NMR (400 MHz, CDCl₃): δ 7.35 (d, J = 7.3 Hz, 2H), 7.25 (q, J = 8.2 Hz, 3H), 7.14 (q, J = 7.3 Hz, 2H), 7.04 (d, J = 8.2 Hz, 1H), 6.94 (s, 1H), 6.86 (t, J = 7.3 Hz, 1H), 3.77 (s, 3H), 1.76 (s, 6H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 150.0, 137.7, 127.9, 126.4, 125.49, 125.46, 124.5, 121.3, 121.1, 118.3, 109.1, 38.9, 32.6, 30.7.

3-(2-Phenylpropan-2-yl)-1H-indole (3m)

Following the general procedure, 3m was obtained as a colorless liquid, 211 mg, 90% yield; ¹H NMR (400 MHz, CDCl₃): δ 7.83 (br s, 1H), 7.35–7.29 (m, 3H), 7.25–7.20 (m, 2H), 7.16–7.03 (m, 4H), 6.86 (t, J = 7.8 Hz, 1H), 1.76 (s, 6H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 149.9, 137.1, 128.0, 126.4, 126.1, 126.0, 125.5, 121.6, 121.3, 120.5, 118.8, 111.0, 38.9, 30.6.

2-Benzhydryl-3-methyl-1H-indole (3n)

Following the general procedure, 3n was obtained as a colorless liquid, 237 mg, 80% yield; ¹H NMR (400 MHz, CDCl₃): δ 7.54 (d, J = 8.7 Hz, 1H), 7.46 (s, 1H), 7.33–7.09 (m, 14H), 5.77 (s, 1H), 2.17 (s, 3H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 142.1, 135.2, 135.1, 129.4, 129.0, 128.7, 126.8, 121.3, 119.2, 118.4, 110.6, 108.2, 48.5, 8.6.

3-Benzhydryl-5-chloro-1H-indole (3o)

Following the general procedure, 3o was obtained as a colorless liquid, 254 mg, 80% yield; ¹H NMR (400 MHz, CDCl₃): δ 7.97 (br s, 1H), 7.30–7.19 (m, 12H), 7.11 (dd, J = 8.2, 1.4 Hz, 1H), 6.58 (s, 1H), 5.60 (s, 1H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 143.5, 135.0, 128.9, 128.4, 128.1, 126.4, 125.4, 125.1, 122.5, 119.7, 119.2, 112.0, 48.5. HRMS (ESI/Q-TOF) m/z: [M – H]⁺ calcd for C₂₁H₁₅ClN 316.0893; found 316.0936.

3-Benzhydryl-5-methoxy-1H-indole (3p)

Following the general procedure, 3p was obtained as a colorless liquid, 260 mg, 83% yield; ¹H NMR (400 MHz, CDCl₃): δ 7.85 (br s, 1H), 7.30–7.20 (m, 11H), 6.82 (dd, J = 8.7, 2.3 Hz, 1H), 6.62 (d, J = 2.3 Hz, 1H), 6.55 (d, J = 1.4 Hz, 1H), 5.61 (s, 1H), 3.65 (s, 3H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 153.7, 143.8, 131.8, 129.0, 128.3, 127.4, 126.2, 124.8, 119.6, 112.1, 111.7, 101.9, 55.8, 48.8. HRMS (ESI/Q-TOF) m/z: [M + H]⁺ calcd for C₂₂H₂₀NO 314.1545; found 314.1538.

3-[(4-Chlorophenyl)(phenyl)methyl]-5-methoxy-1H-indole (3q)

Following the general procedure, 3q was obtained as a colorless liquid, 264 mg, 76% yield; ¹H NMR (400 MHz, CDCl₃): δ 8.07 (br s, 1H), 7.35–7.11 (m, 11H), 6.86 (dd, J = 8.7, 2.3 Hz, 1H), 6.49 (s, 1H), 5.81 (s, 1H), 3.85 (s, 3H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 154.2, 143.4, 142.2, 133.3, 130.9, 130.3, 128.9, 128.63, 128.58, 128.4, 127.9, 126.5, 124.8, 112.3, 111.7, 102.3, 55.8, 48.2. HRMS (ESI/Q-TOF) m/z: [M + H]⁺ calcd for C₂₂H₁₉ClNO 348.1155; found 348.1098.

3-Benzhydryl-5-bromo-1H-indole (3r)

Following the general procedure, 3r was obtained as a colorless liquid, 264 mg, 73% yield; ¹H NMR (400 MHz, CDCl₃): δ 7.96 (br s, 1H), 7.35 (s, 1H), 7.30–7.19 (m, 12H), 6.57 (s, 1H), 5.60 (s, 1H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 143.5, 135.3, 128.9, 128.7, 128.4, 126.4, 125.2, 125.0, 122.3, 119.6, 112.7, 112.5, 48.5.

2-(1-Methyl-1H-indol-3-yl)-1,2-diphenylethan-1-one (3s)

Following the general procedure, 3s was obtained as an orange liquid, 227 mg, 70% yield; ¹H NMR (400 MHz, CDCl₃): δ 8.05 (d, J = 7.3 Hz, 2H), 7.49 (t, J = 7.3 Hz, 2H), 7.38 (t, J = 8.2 Hz, 4H), 7.29 (t, J = 7.3 Hz, 3H), 7.21 (t, J = 6.4 Hz, 2H), 7.07 (t, J = 7.3 Hz, 1H), 6.88 (s, 1H), 6.27 (s, 1H), 3.68 (s, 3H); ¹³C{¹H} NMR (100 MHz, CDCl₃): δ 198.4, 139.1, 137.2, 136.9, 132.9, 129.0, 128.8, 128.6, 128.5, 128.4, 127.0, 121.9, 119.3, 118.8, 112.7, 109.4, 50.5, 32.8. HRMS (ESI/Q-TOF) m/z: [M + H]⁺ calcd for C₂₃H₂₀NO 326.1545; found 326.1525.

Supporting Information Available

The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acsomega.9b01481.

• Copies of ¹H and ¹³C{¹H} NMR and HRMS spectra of the compounds and X-ray crystallographic data (PDF)

• Crystallographic data for 3a (CIF)

Accession Codes

CCDC 1893717 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/data_request/cif, or by emailing data_request@ccdc.cam.ac.uk, or by contacting The Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44 1223 336033.

The authors declare no competing financial interest.