Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8119Generated: October 26, 2026

Bromoacetonitrile → 2-((1H-Indol-4-yl)oxy)acetonitrile

https://huagongshe.com/reaction/8119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetonitrileHCID 11534—
ReactantSodium hydrideHCID 24758—
Reactant1H-indol-4-olHCID 75421—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-((1H-Indol-4-yl)oxy)acetonitrileHCID 1554179997%

Reaction Steps

A 0° C. solution of 4-hydroxyindole (20 g, 150 mmol) in 500 ml of dimethylformamide is treated with NaH (60% dispersion in mineral oil; 6.6 g, 165 mmol). After 30 minutes, bromoacetonitrile (11.5 ml, 165 mmol) is added, and the resulting mixture is allowed to slowly warm to ambient temperature and stir for 3 days. The reaction mixture is diluted with ethyl acetate and washed 3 times with H2O. The organic layer is dried over Na2SO4 and concentrated in vacuo. The crude residue is purified by normal phase HPLC (SiO2; 5% step gradient of 0 to 20% ethyl acetate in hexanes) to give 25 g of (1H-indol-4-yloxy)acetonitrile (97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087635B2
Source datasetuspto-grants-2006_08
ORD IDord-f7a1ba14ffa947f1be82f724f443f402
Source noteuspto-grants-2006_08