Реакция #52343

ord-372f3c86a1f54b10a1e19e5c78854c00

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Экстракцияextracted with diethyl ether (×2)
  2. 2
    ПромывкаThe combined organic phase was washed with water (×1), saturated aqueous sodium bicarbonate (×1) and brine (×1)
  3. 3
    Сушкаdried over anhydrous magnesium sulfate
  4. 4
    Фильтрацияfiltered
  5. 5
    Другоеevaporated 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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06855512B2uspto-grants-2005_02