Reaktion #50162

ord-2f9bf7f3038b4bf7aa5a7d6f8c8af502

Reaktionsgleichung

COc1ccc(O)cc1
4-methoxyphenol
CCCCC(CC)CBr
1-bromo-2-ethylhexane
CCCCC(CC)COc1ccc(OC)cc1
1-methoxy-4-(2'-ethylhexyloxy)benzene
Ausbeute 43.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthis mixture was heated
  2. 2
    Temperaturto reflux for 30 min
  3. 3
    TemperaturThe mixture was then heated
  4. 4
    Temperaturto reflux for 18 hours
  5. 5
    SonstigeThe solvent was removed in vacuo
  6. 6
    workup.DISSOLUTIONthe residue dissolved in ether (200 ml)
  7. 7
    Waschenwashed with dilute aqueous sodium hydroxide (500 ml ) and water (500 ml )
  8. 8
    Trocknendried over MgSO4
  9. 9
    Einengenconcentrated in vacuo again
  10. 10
    workup.DISTILLATIONDistillation at 120° C./0.1 mm Hg

Vorschrift

Sodium metal (6.50 g, 283 mmol) was dissolved in dry methanol (100 ml) under Ar to give a 2.5M solution of sodium methoxide. A solution of 4-methoxyphenol (29.3 g, 236 mmol) in dry methanol (150 ml) was added and this mixture was heated to reflux for 30 min. After cooling to room temperature, a solution of 1-bromo-2-ethylhexane (46.5 g, 259 mmol) in dry methanol (150 ml) was added dropwise. The mixture was then heated to reflux for 18 hours. The solvent was removed in vacuo, the residue dissolved in ether (200 ml), washed with dilute aqueous sodium hydroxide (500 ml ) and water (500 ml ), dried over MgSO4 and concentrated in vacuo again. Distillation at 120° C./0.1 mm Hg afforded 24.2 g (43%) 1-methoxy-4-(2'-ethylhexyloxy)benzene.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05425125uspto-grants-1995_06