Reacción #1820951

ord-2626fbff27c54ab5863bcb45d7601f30

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroimmersed in an ice/water bath
  2. 2
    Otrofitted with an addition funnel
  3. 3
    workup.ADDITIONwas added to the stirred reaction mixture over a period of 45 minutes
  4. 4
    workup.ADDITION3 hrs after the addition
  5. 5
    Otrothe layers were separated
  6. 6
    LavadoThe organic phase was washed with water (250 ml) and brine (250 ml)
  7. 7
    Secadodried (Na2SO4)
  8. 8
    Filtraciónfiltered
  9. 9
    Otroevaporated in vacuo

Procedimiento

A flask containing 10-bromoundecanoic acid (25.0 g, 94.2 mmol) was charged with dry THF (250 ml), immersed in an ice/water bath and fitted with an addition funnel. The addition funnel was charged with borane-THF solution (1.0M, 113 ml, 113 mmol) which was added to the stirred reaction mixture over a period of 45 minutes. 3 hrs after the addition was completed, the reaction was poured into a stirred mixture of EtOAc (500 ml) and 10% aqueous potassium carbonate (300 ml). After vigorously stirring for 0.5 hr, the layers were separated. The organic phase was washed with water (250 ml) and brine (250 ml), dried (Na2SO4), filtered and evaporated in vacuo. Flash column chromatography (silica, 1:4; EtOAc:hexanes) provided 10-bromo-undecan-1-ol (20.8 g, 88%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05531979uspto-grants-1996_07