Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
p-Aminoacetophenone → N-(4-acetylphenyl)methanesulfonamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | p-Aminoacetophenone | HCID 7468 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | N-(4-acetylphenyl)methanesulfonamide | HCID 684083 | 95% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08642657B2 |
| 출처 데이터셋 | uspto-grants-2014_02 |
| ORD ID | ord-ce529ee51da142f182b51d887ecae8d4 |
| 출처 메모 | uspto-grants-2014_02 |