Water → Pyridine, 2-methoxy-4-(trifluoromethyl)-
Reaktionsgleichung
Cl[C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[CH:4][N:3]=1.[CH3:12][O-:13].[Na+].O>CO>[F:9][C:8]([F:11])([F:10])[C:6]1[CH:5]=[CH:4][N:3]=[C:2]([O:13][CH3:12])[CH:7]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution having 5.05 g (27.8 mmol) of 2-chloro-4-trifluoromethylpyridine and 3.59 g (66.5 mmol) of sodium methoxide dissolved in 40 ml of methanol was stirred under reflux with heating for 4 hours. Water was added to terminate the reaction, followed by extraction with diethyl ether. The organic layer was dried over anhydrous sodium sulfate and subjected to filtration on the pad of a silica gel cake. The solvent was distilled off under reduced pressure to obtain 4.19 g (yield: 85%) of 4-trifluoromethyl-2-methoxypyridine.
Aufarbeitung
- temperatureunder reflux
- temperaturewith heating for 4 hours
- customto terminate
- customthe reaction
- extractionfollowed by extraction with diethyl ether
- dry with materialThe organic layer was dried over anhydrous sodium sulfate
- filtrationsubjected to filtration on the pad of a silica gel cake
- distillationThe solvent was distilled off under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-fdb216d1c529489cbb2ed0210183f5ba
- Quelldatensatz
- uspto-grants-2014_02
- Patentnummer
- US08653277B2
Notizen zur Reaktion
Wird geladen…