Reaktion #10020
ord-86800bf9397e44b882523bdaca98c2ce
Reaktionsgleichung
Edukte
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Temperatur
180°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Sonstigeequipped with anchor stirrer
- 2Temperaturthermometer, and reflux condenser
- 3Sonstigewith bubble counter
- 4TemperaturThe mixture was then heated
- 5Temperaturthis temperature was maintained for 16 hours
- 6TemperaturThe mixture was then cooled to room temperature
- 7workup.ADDITIONwater was added to the reaction mixture in a volumetric ratio of 1:1
- 8Extraktionthe mixture was extracted with diethyl ether
- 9WaschenAfter washing
- 10Einengenconcentration
- 11Sonstigedrying the separated organic phase
Vorschrift
200 g of 4-chlorobenzonitrile, 101.4 g of potassium fluoride, 25 g of dimethyl sulfoxide, and 5.60 g of (N,N-dimethylimidazolidino)tetramethyl-guanidinium chloride were placed in a 1 liter 4-neck flask equipped with anchor stirrer, thermometer, and reflux condenser with bubble counter. The mixture was then heated with stirring to 180° C. and this temperature was maintained for 16 hours. The mixture was then cooled to room temperature, water was added to the reaction mixture in a volumetric ratio of 1:1, and the mixture was extracted with diethyl ether. After washing, concentration, and drying the separated organic phase, 4-fluorobenzo-nitrile was isolated in a yield of 75%.