Reaktionsgleichung
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1O.[NH2:12][NH2:13]>>[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[NH:12][NH2:13]Komponenten
3
Reaktionsbedingungen
- Temperatur
- 85 °C
Versuchsvorschrift
57.6 g (0.4 mol) of 2-naphthol and 200 ml of hydrazine (4 mol) are introduced into a 500 ml autoclave. The mixture is stirred at 85° C. at a pressure of 60 bar for approximately 100 hours. The reaction medium is subsequently extracted with dichloromethane. The organic phase is washed with 10% sodium hydroxide, then with water and finally with brine; it is dried over magnesium sulphate. After filtration and evaporation under vacuum, 50.6 g (80%) of product are obtained, the melting point of which is 124° C. (alcohol/water).
Aufarbeitung
- extractionThe reaction medium is subsequently extracted with dichloromethane
- washThe organic phase is washed with 10% sodium hydroxide
- dry with materialit is dried over magnesium sulphate
- filtrationAfter filtration and evaporation under vacuum, 50.6 g (80%) of product
- customare obtained
- customis 124° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-8981c06870b2477f9d10353bdfab6b67
- Quelldatensatz
- uspto-grants-1998_05
- Patentnummer
- US05750722
Verknüpfte Notizen
Wird geladen…