Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711306Generated: October 26, 2026

N-bromobutanimide → (4-Amino-3-bromophenyl)acetonitrile

https://huagongshe.com/reaction/1711306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4-AminophenylacetonitrileHCID 77000—
SolventAcetonitrileHCID 6342—
Product(4-Amino-3-bromophenyl)acetonitrileHCID 4503705392.2%

Reaction Steps

A solution of 4-aminophenylacetonitrile (1.45 g, 10.9 mmol) in acetonitrile (10 mL) at 0° C. was treated with NBS (1.95 g, 10.9 mmol) in acetonitrile (10 mL) dropwise via an addition funnel. The reaction was allowed to warm to room temperature and then concentrated in vacuo. The crude product was dissolved in EtOAc (50 mL), washed with saturated aqueous NaHCO3 (2×50 mL) and dried (Na2SO4). Removal of the solvent in vacuo afforded the title compound (2.12 g, 92%) as a reddish solid. Mass spectrum (ESI, m/z): Calcd. for C8H7BrN2, 210.9 (M+H), found 211.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790724B2
Source datasetuspto-grants-2010_09
ORD IDord-1a9296351bdb408a8b5e398ccc402edd
Source noteuspto-grants-2010_09