Reacción #2307972
ord-5ffa447de9bf44b58e0f6d32b8a07229
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1Temperaturathe reaction mixture was heated
- 2TemperaturaThe reaction mixture was then cooled
- 3Extracciónextracted with methylene chloride (200 ml×2)
- 4LavadoThe combined organic layers were washed with brine once
- 5Secadodried over Na2SO4
- 6Filtraciónfiltered
- 7Concentraciónconcentrated in vacuo to a dark brown oil
- 8OtroThe crude product mixture was purified via flash chromatography (silica gel, gradient elution: ethyl acetate to 9/1 ethyl acetate/methanol)
Procedimiento
An aqueous sodium hydroxide solution prepared by dissolving 3.99 g (100 mmol) NaOH in 4 ml water was added slowly to monodispersed hexaethylene glycol (28.175 g, 25 ml, 100 mmol). Benzyl chloride (3.9 g, 30.8. mmol, 3.54 ml) was added and the reaction mixture was heated with stirring to 100° C. for 18 hours. The reaction mixture was then cooled, diluted with brine (250 ml) and extracted with methylene chloride (200 ml×2). The combined organic layers were washed with brine once, dried over Na2SO4, filtered and concentrated in vacuo to a dark brown oil. The crude product mixture was purified via flash chromatography (silica gel, gradient elution: ethyl acetate to 9/1 ethyl acetate/methanol) to yield 8.099 g (70%) of monodispersed compound 1 as a yellow oil.