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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428738Generated: November 1, 2026

Methanesulfonyl chloride → N-(2-fluoro-4-nitrobenzyl)methanesulfonamide

https://huagongshe.com/reaction/1428738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(2-Fluoro-4-nitrophenyl)methanamineHCID 45121148—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductN-(2-fluoro-4-nitrobenzyl)methanesulfonamideHCID 8667936688.3%

Reaction Steps

To a stirred solution of (2-fluoro-4-nitrophenyl)methanamine (194 mg, 1.140 mmol) in pyridine, cooled to 0° C., were added methanesulfonyl chloride (248 mg, 2.166 mmol). The resulting reaction mixture was stirred for 1 h at room temperature. The mixture was dissolved in dichloromethane and washed with 1N HCl. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. N-(2-Fluoro-4-nitrobenzyl)methanesulfonamide (250 mg) was obtained as 88% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-943dac51f85845d9b70727e7e4d5244d
Source noteuspto-grants-2015_01