HRID403419

反应详情

EQUATION

反应方程式

HRID 403419 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
63 °C

PROCEDURE

实验过程

tert-Butyl 2-amino-5-fluorophenylcarbamate (30.5 g), toluene (300 mL), triethylamine (34.1 g) and ethyl 3,3,3-trifluoro-2-oxopropanoate (69.5 g) were charged into a reactor and warmed to 63° C. for 14 h, then cooled to ambient temperature. A 5% aq. NaOH solution (390 mL) was added, stirred, settled, and then the lower layer was separated. The organic layer extracted with another charge of 5% aq. NaOH solution (130 mL). To the combined aq. NaOH layers was charged 2-methyl-THF (390 mL) and concentrated HCl (77.9 g), keeping the temperature below 25° C. The layers were mixed, settled and separated. The acidic aq. layer was separated, and the organic layer was extracted with water (260 mL). The layers were separated and the organic layer was filtered to remove insoluble material. The product was isolated by switching the solvent to toluene by distillation (a total of 1.1 L toluene used). The final slurry was briefly warmed to 80° C. and then cooled −10° C. and filtered. The cake was washed with toluene (128 mL), then dried under vacuum at 60° C. To the crude solid was added ethanol (350 mL) and warmed to reflux to dissolve the solids. The solution was cooled to room temperature and concentrated to approximately 270 mL total volume by distillation. Water (250 g) was then added over 30 min. The slurry was filtered and washed with cold (1:1) ethanol: water (2×60 mL). The solid was dried under vacuum at 60° C. (26.1 g, 83% yield).

WORKUP

后处理

  1. temperaturecooled to ambient temperature
  2. customthe lower layer was separated
  3. extractionThe organic layer extracted with
  4. additionanother charge of 5% aq. NaOH solution (130 mL)
  5. additionTo the combined aq. NaOH layers was charged 2-methyl-THF (390 mL) and concentrated HCl (77.9 g)
  6. customthe temperature below 25° C
  7. additionThe layers were mixed
  8. customseparated
  9. customThe acidic aq. layer was separated
  10. extractionthe organic layer was extracted with water (260 mL)
  11. customThe layers were separated
  12. filtrationthe organic layer was filtered
  13. customto remove insoluble material
  14. customThe product was isolated
  15. distillationby distillation (a total of 1.1 L toluene
  16. temperatureThe final slurry was briefly warmed to 80° C.
  17. temperaturecooled −10° C.
  18. filtrationfiltered
  19. washThe cake was washed with toluene (128 mL)
  20. customdried under vacuum at 60° C
  21. additionTo the crude solid was added ethanol (350 mL)
  22. temperaturewarmed
  23. temperatureto reflux
  24. dissolutionto dissolve the solids
  25. temperatureThe solution was cooled to room temperature
  26. concentrationconcentrated to approximately 270 mL total volume by distillation
  27. additionWater (250 g) was then added over 30 min
  28. filtrationThe slurry was filtered
  29. washwashed with cold (1:1) ethanol
  30. customThe solid was dried under vacuum at 60° C. (26.1 g, 83% yield)