HRID2051225

反应详情

EQUATION

反应方程式

HRID 2051225 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

A mixture of androst-5-ene-3β,17β-diol diacetate (3.75 g, 10 mmol), dibromantin (2.03 g, 7 mmol), and sodium bicarbonate (4.54 g, 54 mmol) in hexane (200 ml) is heated under reflux for 0.5 hours. The mixture is then cooled and filtered and the filtrate evaporated to dryness. The residue is dissolved in 50 ml toluene and treated with lithium bromide (2 g) in 5 ml of acetone. The mixture is stirred at 0° C. for 2 hours and then treated with 2 ml triethylamine and 1.5 ml benzenethiol. After stirring at room temperature for 1.5 hours, 100 ml ethyl acetate is added and the organic solution is washed with 1 N hydrochloric acid and water. The organic phase is dried and concentrated. The residue is then redissolved in 75 ml ethyl acetate, cooled to 0° C. and treated with 2.6 g of m-chloroperbenzoic acid for 2 hours. The mixture is washed with 10% sodium bicarbonate solution and then concentrated. The residue is dissolved in 100 ml toluene, treated with triethylamine (3.6 ml), heated at 70° C. for 24 hours, cooled, and washed with water. The organic solution was concentrated and chromatographed to yield androst-5,7-diene-3β,17β-diol diacetate. The diacetate is treated with K2CO3 in a 10:1 methanol:water solution overnight to yield, after extractive workup, androst-5,7-diene-3β,17β-diol.

WORKUP

后处理

  1. temperatureis heated
  2. temperatureunder reflux for 0.5 hours
  3. temperatureThe mixture is then cooled
  4. filtrationfiltered
  5. customthe filtrate evaporated to dryness
  6. dissolutionThe residue is dissolved in 50 ml toluene
  7. additiontreated with lithium bromide (2 g) in 5 ml of acetone
  8. additiontreated with 2 ml triethylamine and 1.5 ml benzenethiol
  9. stirringAfter stirring at room temperature for 1.5 hours
  10. addition100 ml ethyl acetate is added
  11. washthe organic solution is washed with 1 N hydrochloric acid and water
  12. customThe organic phase is dried
  13. concentrationconcentrated
  14. dissolutionThe residue is then redissolved in 75 ml ethyl acetate
  15. temperaturecooled to 0° C.
  16. additiontreated with 2.6 g of m-chloroperbenzoic acid for 2 hours
  17. washThe mixture is washed with 10% sodium bicarbonate solution
  18. concentrationconcentrated
  19. dissolutionThe residue is dissolved in 100 ml toluene
  20. additiontreated with triethylamine (3.6 ml)
  21. temperatureheated at 70° C. for 24 hours
  22. temperaturecooled
  23. washwashed with water
  24. concentrationThe organic solution was concentrated
  25. customchromatographed