HRID371060

反应详情

EQUATION

反应方程式

HRID 371060 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a homogeneous solution of 600 mg (1.66 mmole) of 17-(ethylthio)-9-fluoro-11β-hydroxyandrosta-1,4,16-trien-3-one in a mixture of dry dichloromethane (60 ml) and trifluoroacetic acid (207 mg) was added triethylsilane (230 mg) and the mixture was stirred at room temperature under a nitrogen atmosphere for 2.5 hours. Since the tlc of an aliquot showed incomplete reaction, more trifluoroacetic acid (207 mg) and triethylsilane (230 mg) were added. After 1.5 hours the starting material had disappeared by tlc. The resulting solution was diluted with dichloromethane, washed with saturated sodium bicarbonate solution and water, dried (anhydrous sodium sulfate) and evaporated in vacuo to give a solid. This was redissolved in 1:4 hexane chloroform and chromatographed on a 30 g silica gel column. Elution with 1:4 hexane-chloroform, chloroform and 5:95 ethyl acetate-chloroform gave 520 mg of a tlc-homogeneous title compound. Crystallization from acetone-hexane gave 410 mg of an analytical specimen, melting point 223°-225° C., with consistent spectral data.

WORKUP

后处理

  1. additionwere added
  2. waitAfter 1.5 hours the starting material had disappeared by tlc
  3. washwashed with saturated sodium bicarbonate solution and water
  4. dry with materialdried (anhydrous sodium sulfate)
  5. customevaporated in vacuo
  6. customto give a solid
  7. customchromatographed on a 30 g silica gel column
  8. washElution with 1:4 hexane-chloroform, chloroform and 5:95 ethyl acetate-chloroform