Реакция #43938

ord-d925f96ad2644afc88152e75846ea9ee

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Фильтрацияthe insoluble substance was filtered off
  2. 2
    Концентрированиеthe filtrate was concentrated under reduced pressure
  3. 3
    ДругоеThe residue was purified by silica gel column chromatography (ethyl acetate:hexane=0:100-25:75)

Методика

To a solution of 4-bromo-3,5-dimethylphenol (4.02 g, 20.0 mmol), 3-(methylthio)-1-propanol (2.12 g, 20.0 mmol) and tributylphosphine (7.97 mL, 32.0 mmol) in toluene (320 mL) was added 1,1′-(azodicarbonyl)dipiperidine (8.07 g, 32.0 mmol), and the mixture was stirred at room temperature for 18 hr under nitrogen atmosphere. Hexane (160 mL) was added to the reaction mixture, the insoluble substance was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=0:100-25:75) to give the title compound (5.03 g, yield 87%) as a pale-yellow oil.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07732626B2uspto-grants-2010_06