Reacción #11407

ord-dae2fd9bf2a242829a417f449efb103f

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe temperature below 10° C
  2. 2
    FiltraciónThe reaction was filtered through silica gel (2.0 g)
  3. 3
    Lavadowashed with Et2O
  4. 4
    LavadoThe filtrate was washed with H2O saturated aqueous sodium bicarbonate and brine
  5. 5
    SecadoThe organic layer was dried over Na2SO4
  6. 6
    Filtraciónfiltered
  7. 7
    Otroevaporated

Procedimiento

A solution of (2-Benzylsulfanyl)methanol 4 (120 mg, 0.522 mmol) in anhydrous Et2O was cooled to 4° C. A solution of PBr3 (49 μL, 0.52 mmol) in anhydrous Et2O was added dropwise, keeping the temperature below 10° C. The reaction was allowed to warm to ambient temperature and stirred for one hour. The reaction was filtered through silica gel (2.0 g) and washed with Et2O. The filtrate was washed with H2O saturated aqueous sodium bicarbonate and brine. The organic layer was dried over Na2SO4, filtered and evaporated to give 95 mg of the named product as a yellow oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07098223B2uspto-grants-2006_08