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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072614Generated: November 3, 2026

Indole → 1H-Indole-1-acetonitrile

https://huagongshe.com/reaction/1072614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantBromoacetonitrileHCID 11534—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1H-Indole-1-acetonitrileHCID 1223090427.1%

Reaction Steps

A 0° C. solution of indole (7 g, 59.8 mmol) in 200 ml of dimethylformamide is treated with NaH (60% dispersion in mineral oil; 3.1 g, 77.7 mmol). After 20 minutes, bromoacetonitrile (4.2 ml, 59.8 mmol) is added, and the resulting mixture is allowed to slowly warm to ambient temperature and stir overnight. The reaction mixture is diluted with ethyl acetate (500 ml) and washed with H2O (3×200 ml). The organic layer is dried over Na2SO4 and concentrated in vacuo. The crude residue is purified by flash chromatography (SiO2; 5% then 20% ethyl acetate in hexanes) to give 2.53 g of indol-1-yl-acetonitrile (27%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06911463B2
Source datasetuspto-grants-2005_06
ORD IDord-1bd3b4102d7041c39f77b46820cdcbb8
Source noteuspto-grants-2005_06