Reacción #1914825

ord-8cff26140b5e4d72a09b23561c86071f

Ecuación de reacción

B.C1CCOC1
BH3.THF
O=C(O)CCCCCCCCCCCCCCCBr
16-bromohexadecanoic acid
OCCCCCCCCCCCCCCCCBr
desired product
Rendimiento 93.2%
OCCCCCCCCCCCCCCCCBr
16-Bromohexadecan-1-ol
Rendimiento 93.2%

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: US07056669B2uspto-grants-2006_06