反应 #833515

ord-495f487bedfe4f41ae76334d5dcc0546

反应方程式

O=Cc1ccc(O)c(Br)c1
3-Bromo-4-hydroxybenzaldehyde
C=CCBr
allyl bromide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
C=CCOc1ccc(C=O)cc1Br
3-bromo-4-(2-propenyloxy)benzaldehyde

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度After cooling
  2. 2
    过滤the solid was filtered off
  3. 3
    洗涤washed with acetone
  4. 4
    浓缩After complete concentration of the organic phase
  5. 5
    其他there was obtained an oily residue that
  6. 6
    其他was used directly in the second step without further purification

实验过程

3-Bromo-4-hydroxybenzaldehyde (20.1 g, 0.100 mol) and allyl bromide (14.5 g, 0.120 mol) were heated under reflux together with potassium carbonate (20.7 g, 0.150 mol) in 150 ml acetone (abs.) for 8 hours. After cooling, the solid was filtered off and washed with acetone. After complete concentration of the organic phase, there was obtained an oily residue that was used directly in the second step without further purification.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07393367B2uspto-grants-2008_07