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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194722Generated: October 26, 2026

Potassium Iodide → 1-(Bromomethyl)-3-chloro-5-methylbenzene

https://huagongshe.com/reaction/1194722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant3,5-DimethylchlorobenzeneHCID 32887—
ReactantN-bromobutanimideHCID 67184—
CatalystBenzoyl PeroxideHCID 7187—
SolventBenzeneHCID 241—
Product1-(Bromomethyl)-3-chloro-5-methylbenzeneHCID 12375549109.1%

Reaction Steps

A solution of 5-chloro-m-xylene (59.3 g) and dibenzoyl peroxide (5.0 g) in 1.13 L of benzene was heated at reflux. N-Bromosuccinimide (82.2 g) was added in portions over 15 minutes. Heating was continued for an additional 20 minutes until a negative potassium iodide reaction was observed. The reaction mixture was cooled, evaporated and then titurated with hexane (500 ml). The precipitated succinimide was removed by filtration and washed with additional hexane. Concentration afforded 101 g of crude 3-chloro-5-methylbenzyl bromide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816469
Source datasetuspto-grants-1989_03
ORD IDord-1cf85b3a1f3445a68f29f1be99623e2a
Source noteuspto-grants-1989_03