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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 238929Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/238929

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-AminoacetophenoneHCID 7468—
EduktMethanesulfonyl chlorideHCID 31297—
LösungsmittelWaterHCID 962—
LösungsmittelPyridineHCID 1049—
ProduktN-(4-acetylphenyl)methanesulfonamideHCID 68408395%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642657B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-ce529ee51da142f182b51d887ecae8d4
Quellennotizuspto-grants-2014_02