Реакция #4836

ord-30de9da655d044c9895a8b402380e49a

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеA 500 ml polytetrafluoroethylene reactor equipped with stirrer
  2. 2
    Температураthermometer and reflux condenser
  3. 3
    ДругоеThe resultant hydrogen chloride is removed from the reactor through the reflux condenser
  4. 4
    ДругоеExcess hydrogen fluoride is removed by distillation
  5. 5
    workup.DISSOLUTIONthe residue is dissolved in 200 ml of methylene chloride
  6. 6
    Экстракцияthe solution is extracted with water
  7. 7
    ДругоеThe organic phase is separated by distillation

Методика

A 500 ml polytetrafluoroethylene reactor equipped with stirrer, thermometer and reflux condenser is charged with 55.9 g (0.2 mol) of 4-(1,1-dichloro-2,2,2-trifluoroethoxy)chlorobenzene in 100 ml of hydrogen fluoride. 3.0 g (0.01 mol; corresponding to 5 mol%) of antimony pentachloride are added at a temperature in the range from -5° C. to 0° C. The resultant hydrogen chloride is removed from the reactor through the reflux condenser. After 20 minutes at 0° C., the evolution of hydrogen chloride ceases. Excess hydrogen fluoride is removed by distillation, the residue is dissolved in 200 ml of methylene chloride and the solution is extracted with water. The organic phase is separated by distillation, affording 47.3 g (89.8% of theory) of 4-(1-chloro-1,2,2,2-tetrafluoroethoxy)chlorobenzene. Boiling point 181° C., nD25 =1.4362.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04727187uspto-grants-1988_02