Reaktion #1666292
ord-4c7833b96e6c4ea5949923b41a2ddc39
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturwhilst cooling with ice
- 2TemperaturThereafter the reaction mixture is slowly heated to 100°-110°C
- 3Extraktionthe whole is extracted with a mixture of ether and chloroform
- 4WaschenThe organic phase is washed twice with 2 N sodium carbonate solution, three times with 2 N hydrochloric acid and finally once with 2 N sodium carbonate solution
- 5Trocknendried over sodium sulphate
- 6Filtrationfiltered
- 7Sonstigeevaporated
- 8workup.DISTILLATIONThe residue, a brown oil, is distilled in a high vacuum
Vorschrift
33.1 g of β-(m-cyclohexyl-phenyl)-ethanol are mixed with 13.3 ml of absolute pyridine. 12.5 ml of thionyl chloride are added dropwise to this mixture, whilst cooling with ice. Thereafter the reaction mixture is slowly heated to 100°-110°C and is kept at this temperature for 2 hours. The reaction solution is again cooled to room temperature, 29 ml of water are added and the whole is extracted with a mixture of ether and chloroform. The organic phase is washed twice with 2 N sodium carbonate solution, three times with 2 N hydrochloric acid and finally once with 2 N sodium carbonate solution, dried over sodium sulphate, filtered and evaporated. The residue, a brown oil, is distilled in a high vacuum. Hereupon, β-(m-cyclohexyl-phenyl)-ethyl chloride is obtained as a light yellow oil of boiling point 103°-8°C/0.1 mm Hg.