Reacción #1559936

ord-f6fd28a8e9c648ed9a08fe5b3921417c

Ecuación de reacción

C=C(C)CBr
3-bromo-2-methyl-1-propene
CCOC(CCO)OCC
3,3-diethoxy-1-propanol
[H-].[Na+]
sodium hydride
C=C(C)COCCC(OCC)OCC
oil
Rendimiento 50.1%
C=C(C)COCCC(OCC)OCC
3-(3,3-Diethoxypropoxy)-2-methylprop-1-ene
Rendimiento 50.1%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGThe reaction mixture was then stirred for a further 18 hours
  2. 2
    OtroThe reaction mixture was quenched with saturated sodium hydrogen carbonate
  3. 3
    Extracciónextracted with ethyl acetate (×3)
  4. 4
    LavadoThe combined organic extracts were washed with saturated aqueous sodium hydrogen carbonate solution and brine
  5. 5
    Secadodried (sodium sulfate)
  6. 6
    Filtraciónfiltered
  7. 7
    Concentraciónconcentrated under reduced pressure

Procedimiento

To a stirred solution of 3,3-diethoxy-1-propanol (3.0 g, 22.2 mmol) in anhydrous THF (50 mL) was added sodium hydride (60% dispersion in mineral oil, 1.07 g, 26.6 mmol). The reaction mixture was stirred for 30 minutes, and 3-bromo-2-methyl-1-propene (3.63 g, 24.5 mmol) then added. The reaction mixture was then stirred for a further 18 hours. The reaction mixture was quenched with saturated sodium hydrogen carbonate and extracted with ethyl acetate (×3). The combined organic extracts were washed with saturated aqueous sodium hydrogen carbonate solution and brine, dried (sodium sulfate), filtered and concentrated under reduced pressure to afford an oil (2.25 g, 50%). The material used in the next step without further purification.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09012644B2uspto-grants-2015_04