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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646540Generated: October 30, 2026

Carbon Tetrachloride → 4-(Bromomethyl)-3-chlorobenzene-1-sulfonyl chloride

https://huagongshe.com/reaction/1646540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant2-chloro-4-methylbenzenesulfonyl chlorideHCID 289081—
Product4-(Bromomethyl)-3-chlorobenzene-1-sulfonyl chlorideHCID 1938496514%

Reaction Steps

N-Bromosuccinimide (13.76 g, 76 mmol) was added to a stirred solution of 3-chloro-4-toluenesulphonyl chloride (12 g, 76 mmol) in CCl4 (120 ml) under argon. After one hour benzoyl peroxide (0.92 g, 3.8 mmol) was added and the reaction mixture refluxed overnight. The mixture was allowed to cool, the resulting white precipitate filtered off and the filtrate evaporated to a yellow oil. Purification of the residue by chromatography over silica gel (3% ethyl acetate in hexane) afforded 3-chloro-4-bromomethylphenylsulphonyl chloride (3.3 g, 14%) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180723
Source datasetuspto-grants-1993_01
ORD IDord-0e01efa853aa4b73813c2ce72a465057
Source noteuspto-grants-1993_01