Реакция #2328978
ord-9907e12207044518ab4d4b3475823ed4
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1workup.STIRRINGwhile stirring the inner temperature
- 2ТемператураAfter raising the temperature to room temperature
- 3workup.STIRRINGstirring for 2 hours
- 4Другоеterminating
- 5Другоеthe reaction
- 6workup.ADDITIONThe saturated saline was added to the reacted solution
- 7Другоеthe organic layer was separated
- 8Экстракцияthe aqueous layer was extracted with ethyl acetate (twice)
- 9ПромывкаThe combined organic layer was washed with saturated saline
- 10Сушкаdried over anhydrous magnesium sulfate
- 11workup.DISTILLATIONThe solvent was distilled off under reduced pressure
- 12Другоеthe residue was purified by column chromatography
Методика
A THF (180 mL) solution of 60.1 g of a nearly colorless solid obtained in (3-3) was added dropwise in an ethanol (120 mL) solution of 1.65 g of sodium borohydride under stirring at −10° C. while stirring the inner temperature. After raising the temperature to room temperature and stirring for 2 hours, water, ethyl acetate and an aqueous ammonium chloride aqueous were added, thereby terminating the reaction. The saturated saline was added to the reacted solution, and the organic layer was separated, and then the aqueous layer was extracted with ethyl acetate (twice). The combined organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was purified by column chromatography to obtain 15.4 g of trans-4-(trans-4-vinylcyclohexyl)cyclohexylmethanol as a white solid.