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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901154Generated: October 27, 2026

Water → 3-Benzoyloxy-4-chlorobenzyl bromide

https://huagongshe.com/reaction/901154

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 numberUS07361677B2
Source datasetuspto-grants-2008_04
ORD IDord-4579a21d5d1c450ab350e72cee382f06
Source noteuspto-grants-2008_04