Réaction #1519084
ord-9c9d98b4a32842df9bf097386614c7ea
Équation de réaction
Réactifs
Conditions de réaction
Traitement
- 1Températurethe reaction mixture was heated
- 2TempératureThe reaction mixture was then cooled
- 3Extractionextracted with methylene chloride (200 ml×2)
- 4LavageThe combined organic layers were washed with brine once
- 5Séchagedried over Na2SO4
- 6Filtrationfiltered
- 7Concentrationconcentrated in vacuo to a dark brown oil
- 8AutreThe crude product mixture was purified via flash chromatography (silica gel, gradient elution: ethyl acetate to 9/1 ethyl acetate/methanol)
Mode opératoire
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.