Methyl 2-(trifluoromethyl)benzoate → 3-Oxo-3-[2-(trifluoromethyl)phenyl]propanenitrile
Reaktionsgleichung
[NH2:1][C:2]1[CH:6]=CNN=1.CO[C:9](=[O:20])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[C:16]([F:19])([F:18])[F:17]>>[O:20]=[C:9]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[C:16]([F:17])([F:18])[F:19])[CH2:6][C:2]#[N:1]Komponenten
3
Versuchsvorschrift
The product was prepared according to the general procedure for aminopyrazole synthesis (route A1) from 2-trifluoromethyl-benzoic acid methyl ester (3.1 g, 14.0 mmol, 1.0 eq). The crude was precipitated from HCl to give the title product as a yellow solid (2.8 g, yield: 94%).
Aufarbeitung
- customThe product was prepared
- customThe crude was precipitated from HCl
Quellen und Nachweise
- ORD-Eintrag
- ord-e49952edd5b748abaabcd2b8bb4bf5e7
- Quelldatensatz
- uspto-grants-2012_04
- Patentnummer
- US08163729B2
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