Reacción #302896

ord-811825d1797540e0947d913cc770fae5

Ecuación de reacción

O
water
[Li][CH2]CCC
n-butyllithium
CSc1c(F)cccc1C(F)(F)F
1-fluoro-2-methylthio-3-(trifluoromethyl)benzene
O=C=O
carbon dioxide
CSc1c(C(F)(F)F)ccc(C(=O)O)c1F
crude product
CSc1c(C(F)(F)F)ccc(C(=O)O)c1F
2-fluoro-3-methylthio-4-(trifluoromethyl)benzoic acid

Disolventes

Condiciones de reacción

Temperatura
-78°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroexceed −65° C
  2. 2
    Otrodid not exceed −45° C
  3. 3
    TemperaturaThe mixture was then warmed to RT
  4. 4
    Temperaturaonce more cooled to 0° C
  5. 5
    Otroformed
  6. 6
    workup.DISSOLUTIONhad dissolved
  7. 7
    Extracciónthe organic phase was extracted three times with water
  8. 8
    ExtracciónThe aqueous phase was extracted repeatedly with dichloromethane
  9. 9
    Lavadothe combined organic phases were washed with saturated aqueous NaCl solution
  10. 10
    Secadodried over sodium sulfate

Procedimiento

Under an atmosphere of inert gas, 27.5 ml (1.6 M in hexane, 44 mmol) of n-butyllithium were added dropwise to a solution, cooled to −78° C., of 7.98 g (38 mmol) of 1-fluoro-2-methylthio-3-(trifluoromethyl)benzene in 60 ml of anhydrous THF, where the temperature of the reaction mixture should not exceed −65° C. The mixture was stirred at −78° C. for 3 h, and at this temperature a carbon dioxide stream was then introduced such that the temperature of the reaction mixture did not exceed −45° C. The mixture was then warmed to RT and then once more cooled to 0° C. For work-up, water was added dropwise at this temperature until the precipitate formed had dissolved. Diethyl ether was added, and the organic phase was extracted three times with water. The combined aqueous phases were acidified with 10 percent strength hydrochloric acid. The aqueous phase was extracted repeatedly with dichloromethane, the combined organic phases were washed with saturated aqueous NaCl solution and dried over sodium sulfate and the filtrate was then freed from the solvent. The crude product obtained in this manner was then recrystallized from gasoline (80-110° C.)/ethyl acetate. This gave 6.8 g of 2-fluoro-3-methylthio-4-(trifluoromethyl)benzoic acid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08193121B2uspto-grants-2012_06