反应 #42650

反应方程式

(11β,16β)-9-fluoro-11,17-dihydroxy-16-methyl-3,20-dioxopregna-1,4-dien-21-yl acetate

imidazole

trimethylsilyl chloride

→

title compound

收率 103.9%

(11β,16β)-9-fluoro-16-methyl-3,20-dioxo-11,17-bis[(trimethylsilyl)oxy]pregna-1,4-dien-21-yl acetate

收率 103.9%

溶剂

N,N-dimethylformamide

ethyl acetate

反应条件

后处理

1. 1
   洗涤washed successively with water, sat. NH4Cl, water, sat. NaHCO3, water, and brine
2. 2
   干燥The organic phase was dried over Na2SO4
3. 3
   过滤filtered
4. 4
   其他evaporated in vacuo

实验过程

To a solution of (11β,16β)-9-fluoro-11,17-dihydroxy-16-methyl-3,20-dioxopregna-1,4-dien-21-yl acetate (18.79 g, 43.25 mmol) and imidazole (58.89 g, 864.9 mmol) in 200 mL of dry N,N-dimethylformamide was added neat trimethylsilyl chloride (55.0 mL, 433 mmol) dropwise during 15 min. The resulting pale yellow solution was stirred at room temperature for 16 hours. The solution was diluted with ethyl acetate and washed successively with water, sat. NH4Cl, water, sat. NaHCO3, water, and brine. The organic phase was dried over Na2SO4, filtered and evaporated in vacuo to yield 26 g of the title compound as a pale yellow oil.

来源