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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428726Generated: November 1, 2026

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

https://huagongshe.com/reaction/1428726

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 were 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 was removed in vacuo. The crude was purified by column chromatography to give N-(4-bromo-2-fluorobenzyl)methanesulfonamide (7.597 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-fda0fefbfce740f4b2ea26824f85dd6e
Source noteuspto-grants-2015_01