Reacción #2358541

Ecuación de reacción

trifluoroacetic acid

K2CO3

K2CO3

DPPA

3-cyclohexene-1(R)-carboxylic acid

→

N-(Cyclohex-3-en-1(R)-yl)-2,2,2-trifluoro-acetamide

Disolventes

chlorobenzene

triethylamine

chlorobenzene

chlorobenzene

Condiciones de reacción

Tratamiento posterior

1. 1
   Otrothe mixture obtained
2. 2
   workup.ADDITIONwas added dropwise
3. 3
   OtroThe mixture obtained
4. 4
   Temperaturamaintaining the temperature at 80 to 90° C.
5. 5
   Lavadosteady gas evolution and a 20 ml of chlorobenzene line rinse
6. 6
   OtroThe mixture obtained
7. 7
   workup.STIRRINGwas stirred at 78 to 82° C. for 1 h
8. 8
   OtroThe mixture obtained
9. 9
   Temperaturawas cooled to approximately 70° C.
10. 10
    Temperaturamaintaining the temperature at 70 to 80° C.
11. 11
    Lavadoa 25 ml chlorobenzene line rinse
12. 12
    OtroThe mixture obtained
13. 13
    workup.STIRRINGwas stirred at 90 to 95° C. for 2 h
14. 14
    OtroThe mixture obtained
15. 15
    Temperaturawas cooled to 15 to 25° C.
16. 16
    Otrothe mixture obtained
17. 17
    workup.STIRRINGwas stirred for 15 min
18. 18
    OtroThe layers obtained
19. 19
    Otrowere separated and to the upper organic layer
20. 20
    Otroobtained
21. 21
    OtroThe mixture obtained
22. 22
    Filtraciónwas filtered through celite
23. 23
    Otroto remove residual solid
24. 24
    Lavadothe celite was washed with 50 ml of chlorobenzene
25. 25
    OtroThe layers obtained
26. 26
    Otrowere separated
27. 27
    Otroobtained
28. 28
    Extracciónwere back extracted with 250 ml of chlorobenzene
29. 29
    Otrothe combined organic phases obtained
30. 30
    Lavadowere washed with 500 ml of 0.5 M phosphoric acid
31. 31
    OtroThe aqueous layer obtained
32. 32
    Extracciónwas back extracted with 300 ml of chlorobenzene
33. 33
    Otrothe combined organic phases obtained
34. 34
    Lavadowere washed with 500 ml of 5% aqueous NaCl solution

Procedimiento

50 g of 3-cyclohexene-1(R)-carboxylic acid and 425 ml of chlorobenzene were charged to a flask at 20-25° C. and the mixture obtained was stirred. To the mixture obtained 110 ml of triethylamine was added dropwise followed by 25 ml of chlorobenzene. The mixture obtained was warmed to 78 to 82° C. and 109.2 g of DPPA was added in a dose controlled fashion, maintaining the temperature at 80 to 90° C. and steady gas evolution and a 20 ml of chlorobenzene line rinse was given. The mixture obtained was stirred at 78 to 82° C. for 1 h until complete determined by TLC. The mixture obtained was cooled to approximately 70° C. and 226 g of trifluoroacetic acid in 34 ml of chlorobenzene was added dropwise maintaining the temperature at 70 to 80° C., followed by 1.57 g of CuCl and a 25 ml chlorobenzene line rinse. The mixture obtained was stirred at 90 to 95° C. for 2 h and the reaction was followed by TLC until completion. The mixture obtained was cooled to 15 to 25° C. and 375 ml of 20% aqueous K2CO3 solution added and the mixture obtained was stirred for 15 min. The layers obtained were separated and to the upper organic layer obtained was added 375 ml of 20% aqueous K2CO3 solution. The mixture obtained was filtered through celite to remove residual solid and the celite was washed with 50 ml of chlorobenzene. The layers obtained were separated. The combined lower aqueous layers obtained were back extracted with 250 ml of chlorobenzene and the combined organic phases obtained were washed with 500 ml of 0.5 M phosphoric acid. The aqueous layer obtained was back extracted with 300 ml of chlorobenzene and the combined organic phases obtained were washed with 500 ml of 5% aqueous NaCl solution.

Fuente