Reacción #2348098

ord-7613853d66ba438eadd12cc4f30dce05

Ecuación de reacción

CCOc1cc(C)c(OB(O)O)c(F)c1F
compound ( 10 )
CCOc1cc(C)c(OB(O)O)c(F)c1F
2,3-difluoro-4-ethoxy-6-methylphenylboric acid
OO
hydrogen peroxide
[Na]
sodium
Cc1cc(O)c(F)c(F)c1
2,3-difluoro-5-methylphenol

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaUnder cooling with an ice bath
  2. 2
    TemperaturaUnder cooling with an ice bath
  3. 3
    Otroto terminate
  4. 4
    Otrothe reaction
  5. 5
    Extracciónan aqueous layer was extracted with diethyl ether, which
  6. 6
    workup.ADDITIONwas added to the organic layer
  7. 7
    LavadoThe organic layer was washed with a saturated sodium hydrogensufite aqueous solution and saturated saline
  8. 8
    Secadodried over anhydrous magnesium sulfate
  9. 9
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure

Procedimiento

Under cooling with an ice bath, 6.57 g of aqueous hydrogen peroxide was slowly added dropwise to the compound (10) having been dissolved in 37 mL of THF, followed by stirring at room temperature for 3 hours. Under cooling with an ice bath, 20 mL of a saturated sodium hydrogensufite aqueous solution was added thereto to terminate the reaction, and an aqueous layer was extracted with diethyl ether, which was added to the organic layer. The organic layer was washed with a saturated sodium hydrogensufite aqueous solution and saturated saline, and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 3.84 g of 2,3-difluoro-5-methylphenol (11).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07846513B2uspto-grants-2010_12