Реакция #1746

ord-989f1c45e316471198b7f2d873102bdb

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеrises to about 30° C.
  2. 2
    Другоеa substantially homogeneous solution is formed
  3. 3
    Другоеto react for 15 hours at ambient temperature
  4. 4
    ДругоеThe organic phase is separated off
  5. 5
    Экстракцияthe aqueous phase is extracted with methylene chloride again
  6. 6
    ПромывкаThey are washed until neutral,
  7. 7
    Другоеdried
  8. 8
    Другоеevaporated in vacuo
  9. 9
    ДругоеThe yellow oil remaining is crystallised by trituration with diisopropylether
  10. 10
    Другоеthe solid product is recrystallised from diisopropylether
  11. 11
    ДругоеWhite crystals are obtained

Методика

A solution of 24.3 g (0.11 mol) of O-acetyl-4-phenylcyclohexanol in 1300 ml of methylene chloride is combined with 26.0 g (0.86 mol) of paraformaldehyde and 26.0 g (0.19 mol) of zinc chloride. Hydrogen chloride is introduced into this suspension, with stirring, for 2.5 hours, whilst the temperature rises to about 30° C. and a substantially homogeneous solution is formed. The mixture is then allowed to react for 15 hours at ambient temperature and the reaction mixture is then hydrolysed with stirring in about 1.5 litres of ice water. The organic phase is separated off, the aqueous phase is extracted with methylene chloride again and the two organic phases are combined. They are washed until neutral, dried and evaporated in vacuo. The yellow oil remaining is crystallised by trituration with diisopropylether and the solid product is recrystallised from diisopropylether. White crystals are obtained, melting point 87°-89° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05726205uspto-grants-1998_03