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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586613Generated: October 26, 2026

3-Chlorobenzoic Acid → 4-Methylsulphinylphenacyl bromide

https://huagongshe.com/reaction/586613

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chlorobenzoic AcidHCID 447—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-Bromo-1-(4-methylsulfanylphenyl)ethanoneHCID 2737523—
SolventChloroformHCID 6212—
Product4-Methylsulphinylphenacyl bromideHCID 1279553733.2%

Reaction Steps

A solution of 2-bromo-1-(4-methylsulphanylphenyl)-1-ethanone (3.7 g, 15 mmol) in CHCl3 (50 ml) is maintained at a temperature of −5° C. A solution of m-chloroperbenzoic acid (70%, 3.7 g, 15 mmol) in CHCl3 (30 ml) cooled to 0° C. is added dropwise while maintaining an IT of −5° C. to 0° C. After stirring for ½ hour in the cold, the deposited m-chlorobenzoic acid is filtered off. The filtrate is first washed with NaHCO3 solution (8% strength, 50 ml) until acid-free and then rewashed with water (50 ml). The CHCl3 phase dried over Na2SO4 sicc. is concentrated in vacuo. A yellowish residue (1.3 g) results.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936632B2
Source datasetuspto-grants-2005_08
ORD IDord-fd8cd5d0c77a4808bc4768150c663c77
Source noteuspto-grants-2005_08