Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194716Generated: October 31, 2026

N-bromobutanimide → 5-(Bromomethyl)-2-chlorobenzonitrile

https://huagongshe.com/reaction/1194716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Chloro-5-methylbenzonitrileHCID 12557200—
CatalystBenzoyl PeroxideHCID 7187—
SolventBenzeneHCID 241—
Product5-(Bromomethyl)-2-chlorobenzonitrileHCID 1403303530.4%

Reaction Steps

A mixture of 2-chloro-5-methylbenzonitrile (10.6 g, 69.9 mmol), N-bromosuccinimide (12.2 g, 68.5 mmol), and dibenzoyl peroxide (349 mg, 1.44 mmol) in benzene (350 ml) was refluxed 1.5 hours, cooled, and evaporated to dryness under vacuum. The residue was suspended in 7:3 (v/v) hexane-dichloromethane, filtered, and evaporated. The crude product was chromatographed on silica gel (650 g) eluted with 7:3 (v/v) hexane-dichloromethane to provide 4.8 g (30%) 4-chloro-3-cyanobenzyl bromide, m.p. 55°-58° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816469
Source datasetuspto-grants-1989_03
ORD IDord-df76d66bf66e4a0f825f92a8343fa05c
Source noteuspto-grants-1989_03