化工社化工社 化学情報印刷レポート · 研究参考用
p-Aminoacetophenone → N-(4-acetylphenyl)methanesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Aminoacetophenone | HCID 7468 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | N-(4-acetylphenyl)methanesulfonamide | HCID 684083 | 95% |
反応手順
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).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08642657B2 |
| 出典データセット | uspto-grants-2014_02 |
| ORD ID | ord-ce529ee51da142f182b51d887ecae8d4 |
| 出典メモ | uspto-grants-2014_02 |