Reacción #1957260

ord-99d018f0883642f080ebe879afb8155f

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroReaction mixture
  2. 2
    Otroadditional 1 hr
  3. 3
    Otroat RT
  4. 4
    workup.ADDITIONAfter that time the resulted mixture was poured
  5. 5
    workup.STIRRINGwith stirring, into a vessel
  6. 6
    ExtracciónOrganic compounds were extracted with 3×200 ml of ether
  7. 7
    Secadodried over sodium sulfate
  8. 8
    OtroAfter removal of ether material
  9. 9
    workup.DISSOLUTIONwas dissolved in minimum amount of dicloromethane
  10. 10
    Otropurified by silica gel chromatography (100% dicloromethane as eluent)

Procedimiento

Under inert atmosphere 10 ml of BH3.THF complex (1.0 M THF solution) were added to 30 ml THF solution of 2.15 gr (6.41 mmole) of 16-bromohexadecanoic acid at -20° C. Reaction mixture was stirred at this temperature for 2 hrs and then additional 1 hr at RT. After that time the resulted mixture was poured, with stirring, into a vessel containing 200 ml of ice/saturated sodium bicarbonate aqueous solution. Organic compounds were extracted with 3×200 ml of ether. The ether fractions were combined and dried over sodium sulfate. After removal of ether material was dissolved in minimum amount of dicloromethane and purified by silica gel chromatography (100% dicloromethane as eluent). 1.92 gr (93% yield) of the desired product were obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06096273uspto-grants-2000_08