Reacción #61210

ord-9a1a18e3ec1e4a939b1a469a527f0623

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONThe mixture was poured onto water
  2. 2
    Extracciónextracted twice with diethyl ether
  3. 3
    LavadoThe diethyl ether extracts were washed with water and brine
  4. 4
    Secadodried over magnesium sulfate
  5. 5
    Filtraciónfiltered
  6. 6
    Otroevaporated
  7. 7
    Otroto yield a yellow oil
  8. 8
    OtroThe oil was purified by column chromatography
  9. 9
    Lavadoeluting with dichloromethane

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07427682B2uspto-grants-2008_09