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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733512Generated: October 25, 2026

Methanesulfonamide → p-Hexadecylamino-N-(methylsulfonyl)benzamide

https://huagongshe.com/reaction/1733512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonamideHCID 72879—
Reactant4-Hexadecylaminobenzoyl chloride hydrochlorideHCID 13255322—
SolventPyridineHCID 1049—
Productp-Hexadecylamino-N-(methylsulfonyl)benzamideHCID 20437358—

Reaction Steps

A solution of 25.2 g. of 4-(hexadecylamino)benzoyl chloride hydrochloride and 5.8 g. of methanesulfonamide in 250 ml. of pyridine was stirred under reflux for 2 hours and then concentrated in vacuo. The residue was partitioned between water and diethyl ether; the aqueous layer acidified with 1 N HCl, and the organic layer separated, dried (MgSO4), and evaporated. Crystallization of the residual white solid from 60% aqueous acetic acid followed by CH2Cl2 -hexane afforded the product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04242273
Source datasetuspto-grants-1980_12
ORD IDord-015213ca0d38459f99b003e330aa906e
Source noteuspto-grants-1980_12