Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21405Generated: October 26, 2026

Phosphorus tribromide → 4-(2-Bromoethyl)benzonitrile

https://huagongshe.com/reaction/21405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus tribromideHCID 24614—
Reactant4-(2-Hydroxyethyl)benzonitrileHCID 2800815—
SolventCarbon TetrachlorideHCID 5943—
Product4-(2-Bromoethyl)benzonitrileHCID 12886548—

Reaction Steps

A solution of phosphorus tribromide (5 g) in carbon tetrachloride (10 ml) was added, dropwise, to a solution of 4-cyanophenethyl alcohol (8.06 g) in carbon tetrachloride (60 ml). The mixture was heated under reflux for 4 hours. On cooling to room temperature, the mixture was poured onto ice (200 g). The layers were separated and the organic layer was washed with 10% aqueous sodium carbonate (50 ml) and brine (50 ml), dried (MgSO4) and concentrated in vacuo to give a colourless oil which solidified on standing. The solid was chromatographed on silica eluting with ethyl acetate containing hexane (20%). The fractions containing the less polar (higher Rf) product were combined and concentrated in vacuo to give 4-cyanophenethyl bromide as a yellow oil which solidified on standing, yield 8.9 g. The fractions containing the more polar (lower Rf) product were combined and concentrated in vacuo to give the title compound as a colourless solid, yield 0.47 g, m.p. 152°-153° .

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05422358
Source datasetuspto-grants-1995_06
ORD IDord-94cc554d11ba4598bc45790c9073d60b
Source noteuspto-grants-1995_06