Реакция #46030

ord-b88aec028ab3465a9637eaaccef53927

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGby stirring at ambient temperature for 4 hours
  2. 2
    ДругоеAfter terminating
  3. 3
    Другоеthe reaction
  4. 4
    Экстракцияthe aqueous layer was extracted with toluene, which
  5. 5
    workup.ADDITIONwas added to the organic layer
  6. 6
    Промывкаthe organic layer was washed with a saturated salt solution
  7. 7
    Сушкаdried over anhydrous magnesium sulfate
  8. 8
    workup.DISTILLATIONThe solvent was distilled off

Методика

Under a nitrogen atmosphere, 1.52 g of sodium hydride was added to 9.45 g of 2-fluoro-3-((4-propylcyclohexyl)phenyl)phenol (5) dissolved in 60 mL of THF cooling with iced water, and the mixture was stirred at ambient temperature for 30 minutes. 3.07 g of chloromethyl methyl ether was added to the solution under cooling with iced water, followed by stirring at ambient temperature for 4 hours. After terminating the reaction by pouring water into the reaction solution, the aqueous layer was extracted with toluene, which was added to the organic layer, and the organic layer was washed with a saturated salt solution and then dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 11.6 g of 2-fluoro-3-((4-propylcyclohexyl)phenyl)-1-methoxymethoxybenzene (6).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07740769B2uspto-grants-2010_06