Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816271Generated: November 1, 2026

Methylamine → N-methyl-2-nitrobenzene-1-sulfonamide

https://huagongshe.com/reaction/1816271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantDichloromethaneHCID 6344—
Reactant2-Nitrobenzenesulfonyl chlorideHCID 15540—
SolventTetrahydrofuranHCID 8028—
ProductN-methyl-2-nitrobenzene-1-sulfonamideHCID 264906—

Reaction Steps

To a solution of 2-nitrobenzenesulfonyl chloride (25 g, 0.113 mol) and dichloromethane (450 mL) at 4° C. was added dropwise 2M methylamine in tetrahydrofuran (68 mL). The mixture was stirred overnight allowing the ice bath to melt. More 2M methylamine in tetrahydrofuran (97 mL) was added and the reaction was stirred for 1 hour. The reaction mixture was concentrated in vacuo. The residue was dissolved in chloroform (500 mL) and was washed with saturated sodium bicarbonate (250 mL). The aqueous layer was extracted with chloroform (250 mL) and all the chloroform layers combined, dried over sodium sulfate and filtered. The filtrate was concentrated in vacuo and the residue purified by silica gel chromatography using 0-4% methanol in dichloromethane. 22.63 g of N-methyl-2-nitrobenzenesulfonamide was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884801B1
Source datasetuspto-grants-2005_04
ORD IDord-4e6a4e89cb304485baec965320cb4319
Source noteuspto-grants-2005_04