Réaction #302896

Équation de réaction

water

n-butyllithium

1-fluoro-2-methylthio-3-(trifluoromethyl)benzene

carbon dioxide

→

crude product

2-fluoro-3-methylthio-4-(trifluoromethyl)benzoic acid

Solvants

Diethyl ether

THF

Conditions de réaction

Traitement

1. 1
   Autreexceed −65° C
2. 2
   Autredid not exceed −45° C
3. 3
   TempératureThe mixture was then warmed to RT
4. 4
   Températureonce more cooled to 0° C
5. 5
   Autreformed
6. 6
   workup.DISSOLUTIONhad dissolved
7. 7
   Extractionthe organic phase was extracted three times with water
8. 8
   ExtractionThe aqueous phase was extracted repeatedly with dichloromethane
9. 9
   Lavagethe combined organic phases were washed with saturated aqueous NaCl solution
10. 10
    Séchagedried over sodium sulfate

Mode opératoire

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.

Source