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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428722Generated: November 1, 2026

Methanesulfonyl chloride → N-(4-bromo-2-fluorobenzyl)methanesulfonamide

https://huagongshe.com/reaction/1428722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(4-Bromo-2-fluorophenyl)methanamineHCID 3770848—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductN-(4-bromo-2-fluorobenzyl)methanesulfonamideHCID 7084771894.2%

Reaction Steps

To a stirred solution of 4-bromo-2-fluorophenyl-methanamine (5.834 g, 28.592 mmol) in pyridine was added methanesulfonyl chloride (4.2 mL, 54.325 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-bromo-2-fluorobenzyl)methanesulfonamide (7.597 g) was obtained as 93% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-6db461efc2d94a5da7a413f9b4cebbf5
Source noteuspto-grants-2015_01