Hydrazine hydrate (1:1) → HCID 178430911, Verbindung
Reaktionsgleichung
C(O/[CH:4]=[C:5](\[CH3:12])/[C:6](=O)[C:7]([F:10])([F:9])[F:8])C.O.[NH2:14][NH2:15]>CCO>[CH3:12][C:5]1[C:6]([C:7]([F:10])([F:9])[F:8])=[N:14][NH:15][CH:4]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 80 °C
Versuchsvorschrift
Into a 100-mL round-bottom flask, was placed (E)-4-ethoxy-1,1,1-trifluoro-3-methylbut-3-en-2-one (compound 261.1, 2.6 g, 14.3 mmol) in EtOH (20 mL). Hydrazine hydrate (1.8 mL, 38 mmol) was added and the resulting solution was stirred for 2 h at 80° C. The reaction was concentrated under reduced pressure to obtain the title compound as a yellow oil (2 g, crude).
Aufarbeitung
- customInto a 100-mL round-bottom flask, was placed
- concentrationThe reaction was concentrated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-8ee4985915c64c7e9fd2fd372f022501
- Quelldatensatz
- uspto-grants-2016_08
- Patentnummer
- US09428502B2
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