Реакция #65152

ord-fe95702c48d94bb29eb304e32c6b377b

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеsynthesized
  2. 2
    workup.ADDITIONwas added
  3. 3
    ДругоеThe insoluble material was removed by filtration
  4. 4
    Другоеthe solvent was removed by distillation under reduced pressure

Методика

To 1.5 l of diethyl ether was added 12.63 g (33.67 mmol) of 3-bromo-3,4-dihydro-2,2-dimethyl-6-pentafluoroethyl-2H-1-benzopyran-4-ol synthesized according to the process of JP-B-2-237985, and 30.2 g of potassium hydroxide was added thereto, followed by stirring at room temperature for 54 hours. The insoluble material was removed by filtration, and the solvent was removed by distillation under reduced pressure to yield 9.5 g (96.2%) of 3,4-dihydro-2,2-dimethyl-3,4-epoxy-6-pentafluoroethyl-2H-1-benzopyran.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05418232uspto-grants-1995_05