Reaktionsgleichung
[Br:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([NH:8][NH2:9])=[O:7])=[CH:4][CH:3]=1.[C:12](OCC)(OCC)(OCC)[CH3:13]>>[Br:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]2[O:7][C:12]([CH3:13])=[N:9][N:8]=2)=[CH:4][CH:3]=1Komponenten
3
Versuchsvorschrift
A stirred suspension of 4-bromobenzoic hydrazide (4.0 g, 18.6 mmol) in triethyl orthoacetate (15 ml) was heated under reflux for 24 h. The reaction mixture was cooled and the precipitate filtered, washed with 60-80° C. petroleum ether (20 ml) and dried to give the title compound as a yellow solid (3.86 g, 87%).
Aufarbeitung
- temperaturewas heated
- temperatureunder reflux for 24 h
- temperatureThe reaction mixture was cooled
- filtrationthe precipitate filtered
- washwashed with 60-80° C. petroleum ether (20 ml)
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-77deb1aae56a4c75b9cfb0feaa4e0936
- Quelldatensatz
- uspto-grants-2000_04
- Patentnummer
- US06046210
Verknüpfte Notizen
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