Реакция #70367
ord-cfd7f0567da74d15b72aa5d292838452
Реагенты
Нет
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1workup.ADDITIONwas added
- 2Другоеthe mixture was quenched by addition of 40% aqueous NaHSO3 solution
- 3ФильтрацияThe suspension was filtered
- 4Промывкаwashed with H2O
- 5Другоеthe filtrate was freeze-dried
- 6Экстракцияextracted with EtOAc (4×70 mL)
- 7СушкаThe combined organic extracts were dried over Na2SO4
- 8Другоеevaporated to dryness
Методика
To a stirred suspension of 6α-formylandrostane-3,17-dione (1.77 g) in t-ButOH (35 mL) and 5% aqueous Na2HPO4 solution (21.5 mL), 1N aqueous KMnO4 (35 mL) was added. After 5 minutes at room temperature, the mixture was quenched by addition of 40% aqueous NaHSO3 solution. The suspension was filtered, washed with H2O and the filtrate was freeze-dried. The residue was taken up with H2O (50 mL) and extracted with EtOAc (4×70 mL). The combined organic extracts were dried over Na2SO4 and evaporated to dryness to give 6α-carboxyandrostane-3,17-dione (1.80 g, 96%). 1H-NMR (300 MHz, acetone-d6, ppm from TMS): δ 11.99 (1H, bb), 2.46-0.73 (21H, m), 1.01 (3H, s), 0.79 (3H, s).