Trifluoroacetic acid → 2-[4-(trifluoromethyl)-1H-pyrazol-1-yl]acetic acid
Reaktionsgleichung
FC(F)(F)C(O)=O.C([O:12][C:13](=[O:24])[CH2:14][N:15]1[CH:19]=[C:18]([C:20]([F:23])([F:22])[F:21])[CH:17]=[N:16]1)(C)(C)C>C(Cl)Cl>[F:22][C:20]([F:21])([F:23])[C:18]1[CH:17]=[N:16][N:15]([CH2:14][C:13]([OH:24])=[O:12])[CH:19]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 25 °C
Versuchsvorschrift
Trifluoroacetic acid (10 mL) was added to tert-butyl[4-(trifluoromethyl)-1H-pyrazol-1-yl]acetate (Preparation 77, 1.3 g, 5.2 mmol) in dry DCM (10 mL) and the mixture was stirred for 18 hours at 25° C. Then the mixture was evaporated in vacuo and the residue was purified by trituration with diethyl ether:pentane (1:9, 2 mL) to afford the title compound as a white solid (79%, 800 mg).
Aufarbeitung
- customThen the mixture was evaporated in vacuo
- customthe residue was purified by trituration with diethyl ether:pentane (1:9, 2 mL)
Quellen und Nachweise
- ORD-Eintrag
- ord-5357ed14f90d4e139b3d482be45e1b87
- Quelldatensatz
- uspto-grants-2015_10
- Patentnummer
- US09163021B2
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