Reaktionsgleichung
[CH3:1][NH2+:2][CH3:3].[F:4][C:5]([F:15])([F:14])[C:6]1[CH:7]=[C:8]([NH:12][NH2:13])[CH:9]=[CH:10][CH:11]=1.CNC>CCOCC>[F:4][C:5]([F:14])([F:15])[C:6]1[CH:7]=[C:8]([N:12]2[CH:3]=[N:2][CH:1]=[N:13]2)[CH:9]=[CH:10][CH:11]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 60 °C
Versuchsvorschrift
A mixture of 16.4 g of 2A and 17.6 g of 3-trifluoromethylphenylhydrazine were stirred and heated to 60° C. Dimethylamine was evolved in an exothermic reaction and the temperature maintained at 90° C. until evolution ceased (about 30 minutes). After cooling, the reaction mixture was dissolved in ether, washed with water, dried and chromatographically purified to yield 1-(3-trifluoromethylphenyl)-1,2,4-triazole (2B).
Aufarbeitung
- temperaturethe temperature maintained at 90° C. until evolution
- custom(about 30 minutes)
- temperatureAfter cooling
- washwashed with water
- customdried
- customchromatographically purified
Quellen und Nachweise
- ORD-Eintrag
- ord-a74c22ae80eb479b8eb7d28d9fcd5a11
- Quelldatensatz
- uspto-grants-1986_09
- Patentnummer
- US04610717
Verknüpfte Notizen
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