Reaktion #1666292

ord-4c7833b96e6c4ea5949923b41a2ddc39

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwhilst cooling with ice
  2. 2
    TemperaturThereafter the reaction mixture is slowly heated to 100°-110°C
  3. 3
    Extraktionthe whole is extracted with a mixture of ether and chloroform
  4. 4
    WaschenThe 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
  5. 5
    Trocknendried over sodium sulphate
  6. 6
    Filtrationfiltered
  7. 7
    Sonstigeevaporated
  8. 8
    workup.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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US03940434uspto-grants-1976_02