Reacción #2460284

ord-7641f4b513be4a8195275046b45bb342

Ecuación de reacción

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

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe reaction was refluxed under nitrogen
  2. 2
    TemperaturaAfter 5-6 hours of reflux
  3. 3
    Otrothe organic layer was separated
  4. 4
    Secadodried over magnesium sulfate
  5. 5
    Otroevaporated to dryness
  6. 6
    Otroto afford a white fluffy powder

Procedimiento

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%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07459284B2uspto-grants-2008_12