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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280651Generated: October 29, 2026

Benzoyl Peroxide → 4-(4-Chlorobenzoyl)-3,5-dichlorobenzyl bromide

https://huagongshe.com/reaction/280651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant4-(4-Chlorobenzoyl) 3,5-dichlorotolueneHCID 13649651—
SolventBenzeneHCID 241—
Product4-(4-Chlorobenzoyl)-3,5-dichlorobenzyl bromideHCID 1364965635.2%

Reaction Steps

A refluxing solution of 4-(4-chlorobenzoyl)-3,5-dichlorotoluene (7.19 g, 24.0 mmol) and dibenzoylperoxide (370 mg, 1.53 mmol) in benzene (247 ml) was treated in portions with N-bromosuccinimide (7.53 g, 42.3 mmol). The mixture was refluxed 24 hours, cooled, and filtered. The precipitate was washed once with benzene, and the combined filtrate and washings were evaporated under vacuum. The residue was triturated with diethyl ether and filtered, and the filtrate was evaporated under vacuum. The residue was chromatographed on silica gel (500 g) eluted with 7:3 (v/v) n-hexanedichloromethane using a preparative high-performance liquid chromatograph to provide 3.2 g (35%) of 4-(4-chlorobenzoyl)-3,5-dichlorobenzyl bromide, m.p. 69°-73° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04590201
Source datasetuspto-grants-1986_05
ORD IDord-10ef9516df164f2894176c33c1a86856
Source noteuspto-grants-1986_05