HRID2254633

反应详情

EQUATION

反应方程式

HRID 2254633 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

At room temperature, 17.1 g of 17β-acetoxy-17α-methylandrosta-4,6-dien-3-one [U.S. Pat. No. 3,033,752 (1962)] in 170 ml of toluene is combined with 100 ml of diethyl aluminum cyanide solution (1 mole in toluene). After 24 hours, the reaction mixture is introduced into a potassium sodium tartrate solution, diluted with ethyl acetate, and the mixture is stirred for 1 hour at room temperature, extracted with ethyl acetate, the organic phase is washed with water, dried, and concentrate under vacuum. The resultant crude product is allowed to react in 500 ml of methanol at room temperature with 360 mg of potassium carbonate, the mixture is concentrated under vacuum after 2.5 hours, diluted with ethyl acetate, washed with water, and dried. After the crude product has been chromatographed on silica gel with a methylene chloride (tert-butyl methyl ether) gradient, 13 g of 17β-acetoxy-17α-methyl-3-oxoandrost-4-ene-7α-carbonitrile is obtained, mp 211°-216° C. (from isopropyl ether).

WORKUP

后处理

  1. customAt room temperature
  2. extractionextracted with ethyl acetate
  3. washthe organic phase is washed with water
  4. customdried
  5. concentrationconcentrate under vacuum
  6. customto react in 500 ml of methanol at room temperature with 360 mg of potassium carbonate
  7. concentrationthe mixture is concentrated under vacuum after 2.5 hours
  8. additiondiluted with ethyl acetate
  9. washwashed with water
  10. customdried
  11. customAfter the crude product has been chromatographed on silica gel with a methylene chloride (tert-butyl methyl ether) gradient