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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428760Generated: November 2, 2026

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

https://huagongshe.com/reaction/1428760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(2-Methyl-4-nitrophenyl)methanamineHCID 20285976—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductN-(2-methyl-4-nitrobenzyl)methanesulfonamideHCID 8667938938.2%

Reaction Steps

To a stirred solution of (2-methyl-4-nitrophenyl)methanamine (178 mg, 1.071 mmol) in pyridine, cooled to 0° C., were added methane sulfonylchloride (0.16 mL, 2.0349 mmol). The resulting reaction mixture was stirred for 2 h. The mixture 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 to obtain N-(2-methyl-4-nitrobenzyl)methanesulfonamide (100 mg, 38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-2fd1527606ba4919bd226d8bc228d054
Source noteuspto-grants-2015_01