Reacción #2348088

Ecuación de reacción

hydrochloric acid

sec-BuLi

compound ( 2 )

2,3-difluorotoluene

THF

trimethyl borate

THF

→

2,3-difluoro-5-methylphenylboric acid

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.ADDITIONwas added
2. 2
   workup.ADDITIONwas added dropwise
3. 3
   workup.STIRRINGby stirring at the same temperature for 1 hour
4. 4
   workup.STIRRINGstirred over night
5. 5
   TemperaturaUnder cooling with an ice bath
6. 6
   ExtracciónThe aqueous layer was extracted with diethyl ether, which
7. 7
   workup.ADDITIONwas added to the organic layer
8. 8
   Lavadothe organic layer was washed with a saturated saline
9. 9
   Secadodried over anhydrous magnesium sulfate
10. 10
    workup.DISTILLATIONThe solvent was distilled off

Procedimiento

Under a nitrogen atmosphere, 30 g the compound (2) having been dissolved in 240 mL of THF was cooled to −78° C., to which 284 mL of sec-BuLi (1 M/L) was added, followed by stirring at the same temperature for 2 hours. 48.7 g of trimethyl borate having been dissolved in 120 mL of THF was added dropwise thereto at the same temperature, followed by stirring at the same temperature for 1 hour, and the mixture was increased in temperature to room temperature and then stirred over night. Under cooling with an ice bath, 200 mL of 3N hydrochloric acid was added to the mixture. The aqueous layer was extracted with diethyl ether, which was added to the organic layer, and the organic layer was washed with a saturated saline and then dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 48.8 g of 2,3-difluoro-5-methylphenylboric acid (3), which was used in the next step without purification.

Fuente