HRID1742835

反应详情

EQUATION

反应方程式

HRID 1742835 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A mixture of 240.2 g (647 mmol) (ethyl)triphenylphosphonium bromide, 72.5 g (647 mmol) potassium t-butoxide, and toluene (1 L) was stirred at room temperature for 1 hr. Then, 185 g (430 mmol) (3β)-3-[[(1,1,2-trimethylpropyl)dimethylsilyl]-oxy]androsta-5,7-dien-17-one was added with the aid of 50 mL of toluene. The temperature was kept below 25° C. by water cooling. After stirring at room temperature overnight, the reaction was quenched with 24.5 mL (430 mmol) of acetic acid. After stirring for 1 hr, the solid was removed by filtration and washed with 600 mL of toluene. The combined filtrate and washes were concentrated. Then 200 mL of methanol was added and the mixture was concentrated again. The residue was dissolved in a mixture of 650 mL methanol. 65 mL water and 650 mL hexane. The methanol/water layer was back-extracted with 325 mL of hexane. The combined hexane layers were concentrated. Then, 200 mL of methanol was added and the mixture was concentrated again. The resulting solid was suspended in 800 mL of methanol containing 8 mL of triethylamine, and the suspension was refluxed for 30 minutes. After cooling in a refrigerator overnight, the precipitate was filtered, washed with 300 mL of cold methanol, and dried by suction for 4 hr. Further drying at 50° C. under high vacuum afforded, 178.1 g (93.7% yield) of (3β,17Z)-(1,1,2-trimethylpropyl)(pregna-5,7,17(20)-trien-3-yloxy)dimethylsilane as a yellow solid: mp 94°-97° C. [α]D -62.8° (c 0.94, ethanol); Anal. Calcd for C29H48OSi: C, 79.02; H, 10.98; Si, 6.37. Found C, 78.74; H, 11.23; Si, 6.50.

WORKUP

后处理

  1. stirringAfter stirring at room temperature overnight
  2. stirringAfter stirring for 1 hr
  3. customthe solid was removed by filtration
  4. washwashed with 600 mL of toluene
  5. concentrationThe combined filtrate and washes were concentrated
  6. additionThen 200 mL of methanol was added
  7. concentrationthe mixture was concentrated again
  8. dissolutionThe residue was dissolved in a mixture of 650 mL methanol
  9. extractionThe methanol/water layer was back-extracted with 325 mL of hexane
  10. concentrationThe combined hexane layers were concentrated
  11. additionThen, 200 mL of methanol was added
  12. concentrationthe mixture was concentrated again
  13. temperaturethe suspension was refluxed for 30 minutes
  14. temperatureAfter cooling in a refrigerator overnight
  15. filtrationthe precipitate was filtered
  16. washwashed with 300 mL of cold methanol
  17. customdried by suction for 4 hr
  18. customFurther drying at 50° C. under high vacuum
  19. customafforded