Reacción #11004

Ecuación de reacción

4-bromo-3-nitrobenzotrifluoride

triethylamine

methanol

sodium thiomethoxide

water

→

6a

Methyl 2-Methylthio-4-trifluoromethylbenzoate

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.ADDITIONwas added
2. 2
   Otropurged with helium three times and carbon monoxide (CO) four times
3. 3
   Temperaturawas maintained between 50 and 75 psi
4. 4
   workup.ADDITIONby the addition of carbon monoxide as necessary
5. 5
   TemperaturaThe mixture was cooled
6. 6
   workup.DISTILLATIONthe bulk of the solvent was distilled at reduced pressure
7. 7
   workup.ADDITIONWater (10 mL), toluene (15 mL) and 3 N HCl (10 mL) were added
8. 8
   Filtraciónthe mixture was filtered
9. 9
   Otroto remove fine particulates
10. 10
    OtroThe layers were separated
11. 11
    Lavadothe organic layer was washed with aqueous sodium bicarbonate (10 mL)
12. 12
    Otroimmersed in a cool water bath
13. 13
    Otroto consume >95% of 5a
14. 14
    workup.ADDITIONAqueous sodium bicarbonate (10 mL) was added to the reaction mixture
15. 15
    workup.ADDITIONthe layers were then thoroughly mixed
16. 16
    Otroto separate
17. 17
    ExtracciónThe aqueous layer was extracted further with toluene (2×15 mL)
18. 18
    SecadoThe combined organic solution was dried over Na2SO4
19. 19
    Concentraciónconcentrated

Procedimiento

Dichlorobis(triphenylphosphine)palladium (140 mg; 0.20 mmol; 0.01 equiv) was added to a 100-mL autoclave. A mixture of 4-bromo-3-nitrobenzotrifluoride (4a; 3.06 mL; 20 mmol), triethylamine (3.5 mL; 25 mmol; 1.25 equiv), and methanol (60 mL; 75 equiv) was added and the mixture was pressurized and purged with helium three times and carbon monoxide (CO) four times. The reaction mixture was placed under 60 psi carbon monoxide and heated to 100° C. for 6 h. during which time the pressure was maintained between 50 and 75 psi by the addition of carbon monoxide as necessary. The mixture was cooled and vented and the bulk of the solvent was distilled at reduced pressure. Water (10 mL), toluene (15 mL) and 3 N HCl (10 mL) were added and the mixture was filtered to remove fine particulates. The layers were separated and the organic layer was washed with aqueous sodium bicarbonate (10 mL). The organic solution was then added to a mixture of sodium thiomethoxide (1.82 g; 26 mmol; 1.3 equiv) and tetrabutylammonium bromide (0.64 g; 2.0 mmol; 0.10 equiv) dissolved in water (6.85 mL) and immersed in a cool water bath. The reaction mixture was stirred overnight (18 h) at ambient temperature to consume >95% of 5a according to gas chromatography (GC) analysis. Aqueous sodium bicarbonate (10 mL) was added to the reaction mixture and the layers were then thoroughly mixed and allowed to separate. The aqueous layer was extracted further with toluene (2×15 mL). The combined organic solution was dried over Na2SO4 and concentrated to afford 3.71 g of 6a. The crude product was flash-chromatographed and eluted with 1:9 ethyl acetate:heptane to afford 2.71 g (54% overall from 4a) of 6a.

Fuente