HRID72744

反应详情

EQUATION

反应方程式

HRID 72744 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

A mixture of 4-bromo-1-fluoro-2-nitrobenzene 324 mg, ethyl 3-(1H-imidazol-2-yl)propanoate 248 mg, potassium carbonate 407 mg and N,N-dimethylacetamide 10 mL was heated at 100° C. for 12 hours in nitrogen atmosphere. The reaction liquid was diluted with ethyl acetate and water was added thereto to induce phase separation. The organic layer was washed with saturated brine and dried over sodium sulfate, from which then the solvent was distilled off. Thus obtained oily substance was dissolved in a liquid mixture of 10 mL of acetic acid and 10 mL of water, and to the solution 1.51 g of 85% sodium hydrosulfite was added, followed by 2 hours' heating under reflux. The reaction liquid was cooled with ice and neutralized with saturated aqueous sodium hydrogencarbonate solution. Extracting the same with ethyl acetate, the extract was washed with saturated brine, dried over sodium sulfate, and from which the solvent was distilled off. To the resulting oily substance, 358 mg of 1,1′-carbonyldiimidazole and 20 mL of 1,2-dichlorobenzene were added, followed by 5 hours' heating under reflux in nitrogen atmosphere. The solvent was distilled off, and to the residue methanol was added and stirred overnight. Thus precipitated crystals were recovered by filtration, washed with methanol and dried in flowing air to provide 112 mg of the title compound.

WORKUP

后处理

  1. customThe reaction liquid
  2. additionwas added
  3. customphase separation
  4. washThe organic layer was washed with saturated brine
  5. dry with materialdried over sodium sulfate, from which
  6. distillationthe solvent was distilled off
  7. dissolutionThus obtained oily substance was dissolved in a liquid mixture of 10 mL of acetic acid and 10 mL of water
  8. additionto the solution 1.51 g of 85% sodium hydrosulfite was added
  9. temperature' heating
  10. temperatureunder reflux
  11. customThe reaction liquid
  12. extractionExtracting the same with ethyl acetate
  13. washthe extract was washed with saturated brine
  14. dry with materialdried over sodium sulfate
  15. distillationfrom which the solvent was distilled off
  16. additionTo the resulting oily substance, 358 mg of 1,1′-carbonyldiimidazole and 20 mL of 1,2-dichlorobenzene were added
  17. waitfollowed by 5 hours
  18. temperature' heating
  19. temperatureunder reflux in nitrogen atmosphere
  20. distillationThe solvent was distilled off
  21. additionto the residue methanol was added
  22. filtrationThus precipitated crystals were recovered by filtration
  23. washwashed with methanol
  24. customdried