Реакция #2175429
ord-b609f6659a65442991c113ccc80c9af3
Уравнение реакции
Реактанты
Реагенты
Растворители
Условия реакции
Обработка
- 1Температураcooling
- 2Другоеdeposits were removed by filtration through Celite
- 3ЭкстракцияThe filtrate was extracted with ethyl acetate
- 4ПромывкаThe combined organic phase was washed successively with water and brine
- 5Сушкаdried over anhydrous magnesium sulfate
- 6workup.DISTILLATIONThe solvent was distilled off under reduced pressure
- 7Другоеthe residue was purified by recrystallization from heptane
Методика
Lithium aluminum hydride (0.62 g) was suspended in THF (200 ml). 4′-(4-Butoxy-2,3-difluorophenyl)-bicyclohexyl-4-one (s-7) (10.0 g) was added dropwise to the suspension in the temperature range of −20° C. to −10° C., and the stirring was continued in this temperature range for 2 hours. After the completion of the reaction had been confirmed by means of GC analysis, ethyl acetate and then a saturated aqueous solution of ammonia were added to the reaction mixture under ice-cooling and deposits were removed by filtration through Celite. The filtrate was extracted with ethyl acetate. The combined organic phase was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was purified by recrystallization from heptane to give 4′-(4-butoxy-2,3-difluorophenyl)-bicyclohexanol (s-22) (8.8 g). The yield based on the compound (s-7) was 87.5%.