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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19923Generated: October 26, 2026

Water → 3-Benzoyloxy-4-chlorobenzyl bromide

https://huagongshe.com/reaction/19923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant3-Benzoyloxy-4-chlorotolueneHCID 16749222—
SolventDiethyl EtherHCID 3283—
SolventCarbon TetrachlorideHCID 5943—
Product3-Benzoyloxy-4-chlorobenzyl bromideHCID 16747840—

Reaction Steps

A mixture of benzoic acid 2-chloro-5-methyl-phenyl ester (CAB02124, 2.47 g, 10.0 mmol), N-bromo-succinimide (1.96 g, 11.0 mmol) and dibenzoyl peroxide (10 mg) in carbon tetrachloride (25 mL) was heated to reflux for 1 hour (TLC-control). After cooling to room temperature water (50 mL) and diethyl ether (100 mL) were added. The organic layer was separated, washed with brine (20 mL), dried over sodium sulphate and concentrated under reduced pressure. The residue was purified by column chromatography (EtOAc:hexane, 1:40, Rf: 0.21). Yield: 2.012 g (62%) colourless oil, which solidified after a few hours (contains ca. 10% benzoic acid 5-dibromomethyl-2-chloro-phenyl ester).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745472B2
Source datasetuspto-grants-2010_06
ORD IDord-cf649b7a6cbf4902bba31782f4cdf429
Source noteuspto-grants-2010_06