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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361030Generated: October 31, 2026

Water → 1-Benzyl-1H-indole-5-carbonitrile

https://huagongshe.com/reaction/1361030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl ChlorideHCID 7503—
ReactantSodium hydrideHCID 24758—
ReactantIndole-5-carbonitrileHCID 27513—
SolventDimethylformamideHCID 6228—
Product1-Benzyl-1H-indole-5-carbonitrileHCID 1611468398.4%

Reaction Steps

5-Cyanoindole (1.0 g, 7.0 mmol) was dissolved in N,N-dimethylformamide (14 mL) and cooled in an ice-water bath. Sodium hydride (0.31 g, 60%, 7.8 mmol) was added, and the resulting suspension was stirred for 30 min. Benzyl chloride (0.85 mL, 0.94 g, 7.4 mmol) was added, and the cooling was discontinued. The stirring was continued for 65 hours at room temperature. Water (150 mL) was added, and the mixture was extracted with ethyl acetate (3×25 mL). The combined organic phases were washed with brine (30 mL) and dried with sodium sulfate (1 hour). Filtration and concentration yielded the crude material. Purification by flash chromatography on silica gel eluting with ethyl acetate/heptanes=1:3 afforded 1.60 g 1-benzyl-1H-indole-5-carbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879893B2
Source datasetuspto-grants-2011_02
ORD IDord-64f854cb2e3e4171a602c7cf64ebaf36
Source noteuspto-grants-2011_02