Reacción #84018

ord-1c1b134520b04a6899a808cbee763b68

Ecuación de reacción

CCCCCCCCCC=O
decanal
COB(OC)OC
trimethoxyborane
[NH4+].[OH-]
ammonia aqueous
COC(=O)CBr
methyl bromoacetate
CCCCCCCCCC(O)CC(=O)OC
β-hydroxydodecanoic acid methyl ester

Disolventes

Condiciones de reacción

Temperatura
20°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGagitated for ten minutes
  2. 2
    OtroAn organic layer was separated
  3. 3
    Extracciónan aqueous solution layer was extracted two times
  4. 4
    OtroThereafter, the organic solution was collected
  5. 5
    workup.DISTILLATIONA residue thereof was purified by distillation

Procedimiento

6.5 g of zinc, 15.5 g of decanal, 25 ml of trimethoxyborane, and 25 ml of dried THF were put into a 300 ml four-neck round-bottom flask, and 17.5 g of methyl bromoacetate was dripped at 20° C. for two hours in a nitrogen gas stream. After dripping, a resultant thereof was agitated at 20° C. for one hour, and thereafter, 25 ml of saturated ammonia aqueous solution and 25 ml of glycerin were added and agitated for ten minutes. An organic layer was separated and an aqueous solution layer was extracted two times by using diethyl ether. Thereafter, the organic solution was collected and subjected to desolvation. A residue thereof was purified by distillation to obtain a β-hydroxydodecanoic acid methyl ester.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09433211B2uspto-grants-2016_09