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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088833Generated: November 2, 2026

N-Methylcyclohexylamine → N-cyclohexyl-N-methylethenesulfonamide

https://huagongshe.com/reaction/2088833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylcyclohexylamineHCID 7514—
ReactantEthanesulfonylchloride, 2-chloro-HCID 15385—
SolventDichloromethaneHCID 6344—
ProductN-cyclohexyl-N-methylethenesulfonamideHCID 58625116—

Reaction Conditions

Temperature5 °C

Reaction Steps

A mixture of N-methylcyclohexylamine (0.048 mol) and TEA (0.053 mol) in DCM (200 mL) was cooled in an ice bath to 5° C., and then a solution of 2-chloro-ethanesulfonyl chloride (0.048 mol, 97%) in DCM (20 mL) was added dropwise. The reaction mixture was stirred for 2 hours at room temperature and then was washed with H2O. The organic layer was separated, dried (MgSO4), and filtered, and the solvent was evaporated to yield the title compound as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436006B2
Source datasetuspto-grants-2013_05
ORD IDord-e212eabf50a0471494db6cebbfb0f9ed
Source noteuspto-grants-2013_05