Reacción #1559936
ord-f6fd28a8e9c648ed9a08fe5b3921417c
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1workup.STIRRINGThe reaction mixture was then stirred for a further 18 hours
- 2OtroThe reaction mixture was quenched with saturated sodium hydrogen carbonate
- 3Extracciónextracted with ethyl acetate (×3)
- 4LavadoThe combined organic extracts were washed with saturated aqueous sodium hydrogen carbonate solution and brine
- 5Secadodried (sodium sulfate)
- 6Filtraciónfiltered
- 7Concentraciónconcentrated 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.