Reaktionsgleichung
[C:1](#[N:4])[CH:2]=[CH2:3].O.[NH2:6][NH2:7].C(=O)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[CH2:16](O)C>>[NH2:4][C:1]1[N:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[N:6]=[C:3]([CH3:16])[CH:2]=1Komponenten
5
Versuchsvorschrift
A mixture of acrylonitrile (15.3 g, 0.289 mol) and ethanol (75 ml) was stirred in an ice-bath and then hydrazine hydrate (15 ml, 0.3 mol) was added dropwise and the mixture was warmed to room temperature and stirred for 2 hours. Benzaldehyde (30.6 ml, 0.3 mol) was then added and the reaction mixture was stirred at room temperature for about 2 days. The react ion mixture was concentrated in vacuo and the residue was added to a solution of sodium butoxide in butanol [prepared from sodium metal (6.9 g) and butanol (300 ml)]. The reaction mixture was refluxed overnight and then the solvent was concentrated in vacuo to afford 19.4 g of crude 5-amino-1-phenyl methylpyrazole.
Aufarbeitung
- stirringstirred for 2 hours
- stirringthe reaction mixture was stirred at room temperature for about 2 days
- concentrationThe react ion mixture was concentrated in vacuo
- additionthe residue was added to a solution of sodium butoxide in butanol [prepared from sodium metal (6.9 g) and butanol (300 ml)]
- temperatureThe reaction mixture was refluxed overnight
- concentrationthe solvent was concentrated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-50db801540544adb82effaf5be68c7d3
- Quelldatensatz
- uspto-grants-1996_01
- Patentnummer
- US05488055
Verknüpfte Notizen
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