反応 #833515

ord-495f487bedfe4f41ae76334d5dcc0546

反応方程式

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

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

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

実験手順

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.

出典

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