Sodium Hydroxide → 4-(2-Methoxyphenyl)-3-buten-2-one 2-oxime
Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH:9]=[CH:10][C:11](=O)[CH3:12].Cl.[NH2:15][OH:16].[OH-].[Na+]>CO>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH:9]=[CH:10][C:11](=[N:15][OH:16])[CH3:12]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In a 250 ml single neck flask was charged 5.28 g (.30.0 mmoles, 1.0 eq.) of 4-(2-methoxyphenyl)-3-buten-2-one and 5.2 g (75.4 mmoles, 2.5 eq) of hydroxylamine hydrochloride and 6 g of 50% sodium hydroxide (75 mmoles, 2.5 eq) and 100 ml of methanol. The reaction mixture was stirred at reflux for 2 hours. The reaction mixture was concentrated, diluted with water (50 ml), and then extracted with ethyl acetate (2×50 ml). The organic phase was dried and concentrated, to obtain 3.1 g of 4-(2-methoxyphenyl)-3-buten-2-one 2-oxime (E/Z mixture of isomers) as an oil in 54.1% yield.
Aufarbeitung
- temperatureat reflux for 2 hours
- concentrationThe reaction mixture was concentrated
- additiondiluted with water (50 ml)
- extractionextracted with ethyl acetate (2×50 ml)
- customThe organic phase was dried
- concentrationconcentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-dded1130e7554bf282cc88da343269b3
- Quelldatensatz
- uspto-grants-2001_01
- Patentnummer
- US06177462B1
Notizen zur Reaktion
Wird geladen…