反应 #2460284

ord-7641f4b513be4a8195275046b45bb342

反应方程式

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

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The reaction was refluxed under nitrogen
  2. 2
    温度After 5-6 hours of reflux
  3. 3
    其他the organic layer was separated
  4. 4
    干燥dried over magnesium sulfate
  5. 5
    其他evaporated to dryness
  6. 6
    其他to afford a white fluffy powder

实验过程

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%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07459284B2uspto-grants-2008_12