Реакция #2348098

ord-7613853d66ba438eadd12cc4f30dce05

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

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

Методика

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).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07846513B2uspto-grants-2010_12