反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A solution of 33 g (84.09 mmole) of 9-fluoro-16α-methyl-11β,17,21-trihydroxypregna-1,4-diene-3,20-dione in 50% acetic acid (3 liters) was stirred with 320 g of sodium bismuthate at room temperature for 20 hours. The resulting brown suspension was filtered through a bed of deactivated silica powder and washed with 300 ml of 50% acetic acid. The filtrate was concentrated in vacuo to 500 ml, diluted with 250 ml of 20% hydrochloric acid and extracted with chloroform. The chloroform solution was washed with 20% hydrochloric acid and water, dried over anhydrous Na2SO4 and evaporated in vacuo to give a solid. This was dissolved in chloroform and chromatographed on a 250 g-silica gel column, eluting successively with chloroform and 1:4 ethyl acetate-chloroform to give 22.8 g (81.6%) of tlc-homogeneous title compound, melting point 240°-242° with consistent spectral data.
WORKUP
后处理
- filtrationThe resulting brown suspension was filtered through a bed of deactivated silica powder
- washwashed with 300 ml of 50% acetic acid
- concentrationThe filtrate was concentrated in vacuo to 500 ml
- additiondiluted with 250 ml of 20% hydrochloric acid
- extractionextracted with chloroform
- washThe chloroform solution was washed with 20% hydrochloric acid and water
- dry with materialdried over anhydrous Na2SO4
- customevaporated in vacuo
- customto give a solid
- customchromatographed on a 250 g-silica gel column
- washeluting successively with chloroform and 1:4 ethyl acetate-chloroform