Acetic Anhydride → N-(2-(4-Benzoylphenylamino)phenyl)acetamide
反応式
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[NH:8][C:9]1[CH:22]=[CH:21][C:12]([C:13]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[O:14])=[CH:11][CH:10]=1.[C:23](OC(=O)C)(=[O:25])[CH3:24]>>[C:13]([C:12]1[CH:21]=[CH:22][C:9]([NH:8][C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[NH:1][C:23](=[O:25])[CH3:24])=[CH:10][CH:11]=1)(=[O:14])[C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1参加物
3
実験手順
4-(2-Aminophenylamino)benzophenone (Compound 101, 0.58 g, 2 mmol) was dissolved in acetic anhydride (10 ml) and the solution was stirred at room temperature for 3 hours. The precipitate that forms after 75 min was filtered off and washed with water to afford the title compound.
後処理
- waitThe precipitate that forms after 75 min
- filtrationwas filtered off
- washwashed with water
出典と根拠
- ORDレコード
- ord-3626457397764f5681709ebfb618c5cb
- 出典データセット
- uspto-grants-2001_11
- 特許番号
- US06313174B1
反応ノート
読み込み中…