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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23405Generated: October 26, 2026

Water → (5-Nitro-indol-1-yl)-acetonitrile

https://huagongshe.com/reaction/23405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBromoacetonitrileHCID 11534—
Reactant5-NitroindoleHCID 22523—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product(5-Nitro-indol-1-yl)-acetonitrileHCID 2257403697%

Reaction Steps

To a solution of 5-nitroindole (1.62 g, 10 mmole) in DMF (15 ml) was added sodium hydride (60% in oil, 0.440 g, 11 mmole). The reaction mixture was stirred for 30 minutes at room temperature after which time bromoacetonitrile (1.25 g, 10.5 mmole) was added via syringe. After 1 h reaction time at the same temperature, the mixture was poured into 200 ml of water. The precipitate, (5-nitro-indol-1-yl)-acetonitrile, was collected (1.96, 97% yield) and was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852726B2
Source datasetuspto-grants-2005_02
ORD IDord-0736083901cd44039217867a658c9ea8
Source noteuspto-grants-2005_02