Phenacylamine → 2-Aminoacetophenone 4-chlorophenylhydrazone
反応式
[NH2:1][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=O.[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([NH:18][NH2:19])=[CH:14][CH:13]=1>CCO.CC(O)=O.O>[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([NH:18][N:19]=[C:3]([C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH2:2][NH2:1])=[CH:14][CH:13]=1参加物
6
実験手順
A mixture of 10.43 g 2-aminoacetophenone and 11.0 g 4-chlorophenylhydrazine in 30 ml EtOH and 10 ml HOAc was refluxed for one hour. The cooled reaction mixture was diluted with water and the precipitate was collected, washed with water, and dried to give 16.83 g solid. Recrystallization from methanol gave 3.48 g solid, m.p. 109°-112° C.
後処理
- temperaturewas refluxed for one hour
- customThe cooled reaction mixture
- customthe precipitate was collected
- washwashed with water
- customdried
出典と根拠
- ORDレコード
- ord-fd729e02bed74f7e97efb42406945fc6
- 出典データセット
- uspto-grants-1993_05
- 特許番号
- US05214059
反応ノート
読み込み中…