HRID645301

反应详情

EQUATION

反应方程式

HRID 645301 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of 0.5 g of 4-(3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)benzoic acid that was synthesized under Synthetic Example 4 and 0.21 g of 2-picolylamine in 6 mL of N,N-dimethylformamide, 0.32 g of 1-(3-(diethylamino)propyl)-3-ethylcarbodiimide chloride was added at room temperature and the mixture was stirred for 72 hours. After the completion of reaction, 20 mL of ethyl acetate and 15 mL of saturated saline were added to the reaction solution, the mixture was separated to extract an aqueous layer with 10 mL of ethyl acetate whereto an organic layer was added, the resulting mixture was washed with 10 mL of water and dried with anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. After purification of the resulting residue using silica gel column chromatography that was eluted with ethyl acetate-hexane (5:1) to obtain 0.17 g of aimed product as resinous matter.

WORKUP

后处理

  1. additionwas added at room temperature
  2. additionwere added to the reaction solution
  3. customthe mixture was separated
  4. extractionto extract an aqueous layer with 10 mL of ethyl acetate whereto an organic layer
  5. additionwas added
  6. washthe resulting mixture was washed with 10 mL of water
  7. dry with materialdried with anhydrous sodium sulfate
  8. distillationthe solvent was distilled off under reduced pressure
  9. customAfter purification of the resulting residue
  10. washwas eluted with ethyl acetate-hexane (5:1)