Reaktion #1519084

ord-9c9d98b4a32842df9bf097386614c7ea

Reaktionsgleichung

ClCc1ccccc1
Benzyl chloride
[Na+].[OH-]
sodium hydroxide
[Na+].[OH-]
NaOH
OCCOCCOCCOCCOCCOCCO
hexaethylene glycol
OCCOCCOCCOCCOCCOCCOCc1ccccc1
monodispersed compound 1
Ausbeute 70.6%
OCCOCCOCCOCCOCCOCCOCc1ccccc1
Hexaethylene glycol monobenzyl ether
Ausbeute 70.6%

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe reaction mixture was heated
  2. 2
    TemperaturThe reaction mixture was then cooled
  3. 3
    Extraktionextracted with methylene chloride (200 ml×2)
  4. 4
    WaschenThe combined organic layers were washed with brine once
  5. 5
    Trocknendried over Na2SO4
  6. 6
    Filtrationfiltered
  7. 7
    Einengenconcentrated in vacuo to a dark brown oil
  8. 8
    SonstigeThe crude product mixture was purified via flash chromatography (silica gel, gradient elution: ethyl acetate to 9/1 ethyl acetate/methanol)

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07611864B2uspto-grants-2009_11