Reacción #1180079

ord-784af2bb7e3b402e8a89becb53e6f7b4

Ecuación de reacción

OCCCCCCCCCCO
1,10-decanediol
Br
hydrobromic acid
Br
hydrobromic acid
OCCCCCCCCCCBr
10-bromo-1-decanol
Rendimiento 87.0%

Condiciones de reacción

Temperatura
30°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaunder reflux
  2. 2
    workup.WAITthe mixture was boiled for 5 hours
  3. 3
    Otrothe phases were separated
  4. 4
    LavadoThe organic phase was washed first with a solution of 100 g of Na2CO3 in 500 ml of water
  5. 5
    OtroRemoval of the solvent
  6. 6
    LavadoThe byproduct 1,10-dibromodecane was eluted with cyclohexane/diethyl ether (20:1)

Procedimiento

87.8 g (0.50 mol) of 1,10-decanediol, 165.1 g of 48% strength hydrobromic acid and 2.5 l of high-boiling petroleum ether (b.p. 100-140° C.) were heated under reflux with vigorous stirring for 4 hours. A further 80.0 g of 48 strength hydrobromic acid were added, and the mixture was boiled for 5 hours. After cooling to 30° C., the phases were separated. The organic phase was washed first with a solution of 100 g of Na2CO3 in 500 ml of water and then with 2×500 ml of water. Removal of the solvent was followed by chromatography on 700 g of silica gel. The byproduct 1,10-dibromodecane was eluted with cyclohexane/diethyl ether (20:1). Chromatography with cyclohexane/diethyl ether (2:1) afforded 103.9 g (0.44 mol, 87%) of 10-bromo-1-decanol.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08129552B2uspto-grants-2012_03