Реакция #84225

ord-32e2919d73504ab795e3dd1431cbe623

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONThe mixture was poured onto water
  2. 2
    Экстракцияextracted twice with diethyl ether
  3. 3
    ПромывкаThe diethyl ether extracts were washed with water and brine
  4. 4
    Сушкаdried over magnesium sulfate
  5. 5
    Фильтрацияfiltered
  6. 6
    Другоеevaporated
  7. 7
    Другоеto yield a yellow oil
  8. 8
    ДругоеThe oil was purified by column chromatography
  9. 9
    Промывкаeluting with dichloromethane

Методика

1-Ethylsulfanyl-2-methyl-but-3-yn-2-ol (0.29 g, 2.0 mmol) was added to a mixture of sodium hydride (60% dispersion in mineral oil, 88 mg, 2.2 mmol) in dimethylformamide (5 mL) under argon. Iodomethane (0.12 mL, 2.0 mmol) was then added to the reaction mixture via syringe and the mixture allowed to stir overnight. The mixture was poured onto water and extracted twice with diethyl ether. The diethyl ether extracts were washed with water and brine, dried over magnesium sulfate, filtered, and evaporated to yield a yellow oil. The oil was purified by column chromatography eluting with dichloromethane to yield the title compound as a clear liquid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09434688B2uspto-grants-2016_09