Реакция #52343
ord-372f3c86a1f54b10a1e19e5c78854c00
Уравнение реакции
Реактанты
Реагенты
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Экстракцияextracted with diethyl ether (×2)
- 2ПромывкаThe combined organic phase was washed with water (×1), saturated aqueous sodium bicarbonate (×1) and brine (×1)
- 3Сушкаdried over anhydrous magnesium sulfate
- 4Фильтрацияfiltered
- 5Другоеevaporated in vacuo
Методика
A solution of 7-methoxy-1,1-dimethyl-1,2,3,4-tetrahydronaphthalene (Intermediate 8, 1.65 g, 8.7 mmol) in 7.5 mL of glacial acetic acid was cooled to 0° C. and treated with a solution of chromium trioxide (2 g, 20 mmol) in 8mL of acetic acid and 7 mL of water. The reaction mixture was then allowed to warm to ambient temperature and stirred overnight. It was diluted with water and extracted with diethyl ether (×2). The combined organic phase was washed with water (×1), saturated aqueous sodium bicarbonate (×1) and brine (×1), dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to afford the title compound (1.64 g, 93%) as a yellow oil.