Réaction #1914825

ord-8cff26140b5e4d72a09b23561c86071f

Équation de réaction

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

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07056669B2uspto-grants-2006_06