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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246232Generated: October 26, 2026

Methanesulfonyl chloride → N-(3-chloro-4-cyanophenyl)methanesulfonamide

https://huagongshe.com/reaction/2246232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-2-chlorobenzonitrileHCID 88728—
SolventDichloromethaneHCID 6344—
ProductN-(3-chloro-4-cyanophenyl)methanesulfonamideHCID 669685—

Reaction Steps

To a stirred solution of 4-amino-2-chlorobenzonitrile (5.02 g, 32.9 mmol) in dichloromethane (80 mL) was added N,N-diisopropylethylamine (17.0 mL, 97.8 mmol) and methanesulfonyl chloride (3.0 mL, 38.8 mmol) at −78° C. The reaction was then allowed to warm to room temperature slowly. After stirring at room temperature for 12 h, the reaction was quenched with 1 N hydrochloric acid. The organic phase was concentrated in vacuo and the residue was purified by flash chromatography (silica gel, 50:50 hexanes/ethyl acetate) to give the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687492B2
Source datasetuspto-grants-2010_03
ORD IDord-e2b8e8572112476fb1d7d958a2cd6615
Source noteuspto-grants-2010_03