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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414142Generated: October 31, 2026

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

https://huagongshe.com/reaction/2414142

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 numberUS04721791
Source datasetuspto-grants-1988_01
ORD IDord-9b8704a1b48d4b38a3f7d6ac01b980f9
Source noteuspto-grants-1988_01