HRID1708748

反应详情

EQUATION

反应方程式

HRID 1708748 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 11.6 mg (0.0112 mmole) of tris(dibenzylideneacetone)dipalladium(chloroform), 22.4 μl (0.0898 mmole) of tributylphosphine and 2 ml of dry tetrahydrofuran was stirred in an atmosphere of argon gas at room temperature for 10 minutes. To this mixture was added 14.2 mg (0.224 mmole) of ammonium formate, followed by stirring for 30 minutes. To the resulting mixture was further added a solution of 27.3 mg (0.0561 mmole) of 20-(5,5-dimethyl-1,3-dioxan-2-yl)-1α,2α;6α,7α-diepoxypregn-4-en-3β-yl acetate in 2 ml of dry tetrahydrofuran and the mixture was refluxed for 10 minutes. The reaction mixture was cooled to room temperature, diluted with methylene chloride and washed with cold 1N-hydrochioric acid. The aqueous layer (washings) was extracted with methylene chloride and the extract was combined with the organic layer. The resulting mixture was washed successively with cold saturated aqueous sodium hydrogen carbonate solution and aqueous sodium chloride solution and dried over magnesium sulfate. The solvent was then distilled off under reduced pressure. Purification of the residue by silica gel chromatography (eluent: ethyl acetate-hexane=1:5, v/v) gave 11.0 mg of 20-(5,5-dimethyl-1,3-dioxan-2-yl)-1α,2α-epoxy-7α-hydroxypregn-5-en-3β-yl acetate (yield: 40%). In addition, 11.8 mg of 20-(5,5-dimethyl-1,3-dioxan-2-yl )-1α,2α-epoxy-7α-hydroxypregn-4-en-3β-yl acetate was recovered as a byproduct (yield: 43%).

WORKUP

后处理

  1. stirringby stirring for 30 minutes
  2. additionTo the resulting mixture was further added a solution of 27.3 mg (0.0561 mmole) of 20-(5,5-dimethyl-1,3-dioxan-2-yl)-1α,2α
  3. temperatureThe reaction mixture was cooled to room temperature
  4. washwashed with cold 1N-hydrochioric acid
  5. extractionThe aqueous layer (washings) was extracted with methylene chloride
  6. washThe resulting mixture was washed successively with cold saturated aqueous sodium hydrogen carbonate solution and aqueous sodium chloride solution
  7. dry with materialdried over magnesium sulfate
  8. distillationThe solvent was then distilled off under reduced pressure
  9. customPurification of the residue by silica gel chromatography (eluent