Reacción #324681

ord-ef70e29ed21546b2a8527d437f2c62ee

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónthe mixture extracted with diethyl ether
  2. 2
    LavadoThe organic layer is washed with brine
  3. 3
    Secadodried (Na2SO4)
  4. 4
    Otrovolatiles removed under reduced pressure

Procedimiento

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).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08642585B2uspto-grants-2014_02