Acetic Acid → 6-(2-Hydroxyphenyl)-3(2H)-pyridazinone
Reaktionsgleichung
O[CH:2]([CH2:6][C:7](=O)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[OH:14])[C:3](O)=[O:4].[NH3:16].[NH2:17]N.C(O)(=O)C>O>[OH:14][C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=1[C:7]1[CH:6]=[CH:2][C:3](=[O:4])[NH:16][N:17]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a stirred suspension of 2-hydroxy-4-oxo-4-(2-hydroxyphenyl)butyric acid in water was added ammonia until pH 7.0 was attained. Hydrazine was added slowly with the concurrent addition of sufficient glacial acetic acid to maintain a pH of 7.0. Steam heating was applied for 2 hours and during this time the pH of 7.0 was maintained by the addition of ammonia as necessary. The reaction mixture was allowed to cool to room temperature. The solid was filtered off, washed with water, 2-propanol and dried (MgSO4) to afford 6-(2-hydroxyphenyl)-3(2H)-pyridazinone (85%).
Aufarbeitung
- temperatureto maintain a pH of 7.0
- temperatureSteam heating
- filtrationThe solid was filtered off
- washwashed with water, 2-propanol
- dry with materialdried (MgSO4)
Quellen und Nachweise
- ORD-Eintrag
- ord-caf4335781aa4d75bb4cdf7359c0a5b8
- Quelldatensatz
- uspto-grants-1985_07
- Patentnummer
- US04528371
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