HRID13349

反应详情

EQUATION

反应方程式

HRID 13349 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

PROCEDURE

实验过程

1 ml of water and 600 mg of iodine were added to a tetrahydrofuran (4 ml) solution of 200 mg of N-(1-(2-fluoro-4-nitro-phenyl)-3-butenyl)-acetamide, and the reaction liquid was stirred overnight at room temperature. The reaction liquid was diluted with chloroform, washed with aqueous saturated sodium bicarbonate, aqueous saturated sodium thiosulfate and saturated saline in order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure to obtain a crude product. 0.25 ml of triethylamine, 0.13 ml of acetic anhydride and 10 mg of 4-dimethylaminopyridine were added to a chloroform (5 ml) solution of the crude product, and the reaction liquid was stirred at room temperature for 15 minutes. The solvent was evaporated away under reduced pressure, 20 mg of potassium carbonate was added to a methanol (5 ml) solution of the resulting residue, and the reaction liquid was stirred at room temperature for 15 minutes. The solvent was evaporated away under reduced pressure, and the residue was purified through silica gel column chromatography (developing solvent: chloroform/methanol=30/1) to obtain the entitled compound as a colorless solid diastereomer mixture.

WORKUP

后处理

  1. customthe reaction liquid
  2. customThe reaction liquid
  3. washwashed with aqueous saturated sodium bicarbonate, aqueous saturated sodium thiosulfate and saturated saline in order
  4. dry with materialdried with anhydrous sodium sulfate
  5. customThe solvent was evaporated away under reduced pressure
  6. customto obtain a crude product
  7. customthe reaction liquid
  8. stirringwas stirred at room temperature for 15 minutes
  9. customThe solvent was evaporated away under reduced pressure, 20 mg of potassium carbonate
  10. additionwas added to a methanol (5 ml) solution of the resulting residue
  11. customthe reaction liquid
  12. stirringwas stirred at room temperature for 15 minutes
  13. customThe solvent was evaporated away under reduced pressure
  14. customthe residue was purified through silica gel column chromatography (developing solvent: chloroform/methanol=30/1)