Reacción #1265351

ord-8cb02306211f4440925d4e1877afe1c7

Ecuación de reacción

CC(C)(C)OC(=O)CBr
Bromoacetic acid tert-butyl ester
COCCOCCOCCO
triethylene glycol monomethyl ether
Cc1ccccc1
toluene
[K+].[OH-]
KOH
COCCOCCOCCCOCC(=O)OC(C)(C)C
CH3(OCH2CH2)3CH2OCH2CO2C(CH3)3
Rendimiento 12.0%

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe reaction mixture was warmed to ambient temperature
  2. 2
    workup.STIRRINGstirred for 1 h
  3. 3
    Otrothe organic layer was separated
  4. 4
    LavadoThe organic layer was washed with saturated aq. NH4Cl (2×100 mL), saturated aq. NaHCO3 (100 mL), brine (100 mL)
  5. 5
    Secadodried over anhydrous MgSO4
  6. 6
    ConcentraciónThe solution was concentrated in vacuo
  7. 7
    Lavadoeluted with ethyl acetate

Procedimiento

Bromoacetic acid tert-butyl ester (20 mL, 0.14 mol), was added over a 10 min period to a rapidly stirred mixture of triethylene glycol monomethyl ether (20 mL, 0.13 mol), tetrabutyl ammonium bromide (20 g, 0.062 mol), toluene (100 mL) and KOH (50% w/w, 100 mL), and the resulting heterogeneous reaction mixture was stirred at 0° C. for 10 min. The reaction mixture was warmed to ambient temperature and stirred for 1 h. Water (100 mL) was added and the organic layer was separated. The organic layer was washed with saturated aq. NH4Cl (2×100 mL), saturated aq. NaHCO3 (100 mL), brine (100 mL), and dried over anhydrous MgSO4. The solution was concentrated in vacuo and the residue was loaded onto a silica gel gravity column (200 g) and eluted with ethyl acetate to afford CH3(OCH2CH2)3CH2OCH2CO2C(CH3)3 as a colorless oil (420 g, 12%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07276286B2uspto-grants-2007_10