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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238929생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/238929

반응식

참여 물질

역할이름HCID투입량
반응물p-AminoacetophenoneHCID 7468—
반응물Methanesulfonyl chlorideHCID 31297—
용매WaterHCID 962—
용매PyridineHCID 1049—
생성물N-(4-acetylphenyl)methanesulfonamideHCID 68408395%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642657B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-ce529ee51da142f182b51d887ecae8d4
출처 메모uspto-grants-2014_02