Реакция #822584
ord-c97fbbf913d5484485f5b1ef6ca95312
Уравнение реакции
Реагенты
Нет
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Другоеquenched
- 2workup.ADDITIONby cautiously adding an ice-water mixture
- 3ДругоеThe organic phase was removed
- 4Экстракцияthe aqueous phase extracted with ethyl acetate (3×200 ml)
- 5ПромывкаThe combined organic phases were washed with water (600 ml) and saturated sodium chloride solution (600 ml)
- 6Сушкаdried over sodium sulphate
- 7Концентрированиеconcentrated under reduced pressure
Методика
A solution of methyl 7-oxanorborn-2-en-5-ylcarbonate (16.163 g, 105 mmol, see Example 1) in THF (75 ml) was added dropwise with stirring and under nitrogen to a suspension of lithium aluminium hydride (4.376 g, 115 mmol) in anhydrous THF (100 ml), in such a way that the solution boiled gently. The reaction mixture was subsequently stirred at room temperature for another 12 h and then quenched by cautiously adding an ice-water mixture. The organic phase was removed and the aqueous phase extracted with ethyl acetate (3×200 ml). The combined organic phases were washed with water (600 ml) and saturated sodium chloride solution (600 ml), dried over sodium sulphate and concentrated under reduced pressure.