Реакция #324681

ord-ef70e29ed21546b2a8527d437f2c62ee

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Экстракцияthe mixture extracted with diethyl ether
  2. 2
    ПромывкаThe organic layer is washed with brine
  3. 3
    Сушкаdried (Na2SO4)
  4. 4
    Другоеvolatiles removed under reduced pressure

Методика

3-Bromo-2-methylphenol (0.10 g), 3-(methylthio)propanol (0.055 mL), tri-n-butyl phosphine (0.12 g) and 1,1′-(azodicarbonyl)dipiperidine (0.15 g) are stirred in tetrahydrofurane for 16 hours. Water is added and the mixture extracted with diethyl ether. The organic layer is washed with brine, dried (Na2SO4) and volatiles removed under reduced pressure. The product (80 mg) is obtained after column chromatography (silica gel, n-hexane/ethyl acetate gradient 100:0 to 50:50).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08642585B2uspto-grants-2014_02