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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280639Generated: October 31, 2026

N-bromobutanimide → 4-(4-Chlorobenzoyl)-3-chlorobenzyl bromide

https://huagongshe.com/reaction/280639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4-(4-Chlorobenzoyl)-3-chlorotolueneHCID 13649649—
CatalystBenzoyl PeroxideHCID 7187—
SolventBenzeneHCID 241—
Product4-(4-Chlorobenzoyl)-3-chlorobenzyl bromideHCID 1364965449.2%

Reaction Steps

A stirred refluxing solution of 4-(4-chlorobenzoyl)-3-chlorotoluene (2.65 g, 9.99 mmol) and dibenzoylperoxide (100 mg, 0.413 mmol) in benzene (100 ml) was treated in portions with an intimate mixture of N-bromosuccinimide (2.2 g, 12. mmol) and dibenzoylperoxide (100 mg, 0.413 mmol). The mixture was refluxed 1.5 hours, cooled, and filtered. The filtrate was evaporated under vacuum, triturated with diethyl ether (100 ml), and filtered. The filtrate was evaporated under vacuum and the residue was chromatographed on silica gel (500 g) eluted with 97:3 (v/v) n-hexane-ethyl acetate using a preparative highperformance liquid chromatograph to provide 1.69 g (49%) of 4-(4-chlorobenzoyl)-3-chlorobenzyl bromide, m.p. 88°-90° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04590201
Source datasetuspto-grants-1986_05
ORD IDord-f82d02ae12bd4e0cbd96e9329d9ca9e1
Source noteuspto-grants-1986_05