Reaktionsgleichung
[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]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 75 °C
Versuchsvorschrift
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.
Aufarbeitung
- customThe addition product precipitated out of the reaction mixture
- temperatureThe mixture was chilled in ice
- filtrationfiltered
- washThe solid was washed with ether
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-f5448ce8bb464f0f984124114fd2fa26
- Quelldatensatz
- uspto-grants-1977_06
- Patentnummer
- US04030925
Verknüpfte Notizen
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