Réaction #2460284

ord-7641f4b513be4a8195275046b45bb342

Équation de réaction

Oc1ccc(Br)cc1
4-Bromophenol
O=C([O-])[O-].[K+].[K+]
potassium carbonate
BrCc1ccccc1
benzyl bromide
Brc1ccc(OCc2ccccc2)cc1
4-benzyloxybromobenzene

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe reaction was refluxed under nitrogen
  2. 2
    TempératureAfter 5-6 hours of reflux
  3. 3
    Autrethe organic layer was separated
  4. 4
    Séchagedried over magnesium sulfate
  5. 5
    Autreevaporated to dryness
  6. 6
    Autreto afford a white fluffy powder

Mode opératoire

4-Bromophenol (2 g, 0.0116 mol) in acetone (40 ml) was treated with potassium carbonate (1.91 g, 1.2 equivalents) and benzyl bromide (1.44 ml, 1.05 equivalents). The reaction was refluxed under nitrogen. After 5-6 hours of reflux, the reaction was cooled to room temperature and diluted with an equal volume of ethyl acetate. This was diluted further with water and the organic layer was separated, dried over magnesium sulfate and evaporated to dryness to afford a white fluffy powder. Yield=2.36 g (73%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07459284B2uspto-grants-2008_12