反応式
[C:1]([NH:4][NH:5][C:6]1[CH:11]=[CH:10][C:9]([NH2:12])=[CH:8][CH:7]=1)(=[O:3])[CH3:2].[CH:13](=O)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>C(O)C>[C:1]([NH:4][NH:5][C:6]1[CH:11]=[CH:10][C:9]([N:12]=[CH:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[CH:8][CH:7]=1)(=[O:3])[CH3:2]参加物
4
反応条件
- 温度
- 75 °C
実験手順
1-Acetyl-2-(4-aminophenyl)hydrazine (8.25 g, 0.05 mole) and benzaldehyde (5.3 g, 0.05 mole) were mixed in ethanol (50 ml). The mixture was stirred thoroughly and was warmed to approximately 75° C for one-half hour. The addition product precipitated out of the reaction mixture. The mixture was chilled in ice and then filtered. The solid was washed with ether and dried. The product was a white crystalline powder. Yield 12.0 g (94%), m.p. 172°-174° C.
後処理
- customThe addition product precipitated out of the reaction mixture
- temperatureThe mixture was chilled in ice
- filtrationfiltered
- washThe solid was washed with ether
- customdried
出典と根拠
- ORDレコード
- ord-f5448ce8bb464f0f984124114fd2fa26
- 出典データセット
- uspto-grants-1977_06
- 特許番号
- US04030925
関連ノート
読み込み中…