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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428712Generated: November 2, 2026

Methanesulfonyl chloride → N-[(4-bromophenyl)methyl]methanesulfonamide

https://huagongshe.com/reaction/1428712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-BromobenzylamineHCID 77571—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductN-[(4-bromophenyl)methyl]methanesulfonamideHCID 1902742395.1%

Reaction Steps

To a stirred solution of (4-bromophenyl)methanamine (500 mg, 2.687 mmol) in pyridine were added methanesulfonyl chloride (0.4 mL, 5.106 mmol) at 0° C. The reaction mixture was stirred for 1 h, then diluted with dichloromethane. The mixture was washed with water. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. N-(4-bromobenzyl)methane-sulfonamide (675 mg) was obtained in 95% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-be99fc43f0034857942c2e7984969292
Source noteuspto-grants-2015_01