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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238929Generated: October 25, 2026

p-Aminoacetophenone → N-(4-acetylphenyl)methanesulfonamide

https://huagongshe.com/reaction/238929

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-AminoacetophenoneHCID 7468—
ReactantMethanesulfonyl chlorideHCID 31297—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductN-(4-acetylphenyl)methanesulfonamideHCID 68408395%

Reaction Steps

A cooled solution of 4′-aminoacetophenon (10 mmol) in pyridine (10 mL) at 0° C. was treated with methanesulfonyl chloride (15 mmol) and stirred at room temperature for 2 h. The reaction mixture was diluted with H2O and extracted with EtOAc several times. The combined organic layers were washed with H2O and brine, dried over MgSO4, filtered, and the filtrate was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel using EtOAc:hexanes to afford 4′-(Methylsulfonylamino)acetophenone (13-5, LJO-298).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642657B2
Source datasetuspto-grants-2014_02
ORD IDord-ce529ee51da142f182b51d887ecae8d4
Source noteuspto-grants-2014_02