反応 #3121

ord-db854b27d2914399bbe5f288a9a9adb4

反応方程式

O=Cc1ccc(O)cc1
4-hydroxybenzaldehyde
BrCCCBr
1,3-dibromopropane
O=Cc1ccc(OCCCOc2ccc(C=O)cc2)cc1
product
収率 76.0%
O=Cc1ccc(OCCCOc2ccc(C=O)cc2)cc1
1,3-bis(4-formyl-phenoxy)propane
収率 76.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度under reflux
  2. 2
    workup.ADDITIONThe reaction mixture was poured
  3. 3
    workup.DISTILLATIONinto cold distilled water
  4. 4
    その他to obtain a precipitate
  5. 5
    ろ過After filtration and vacuum
  6. 6
    その他drying the precipitate
  7. 7
    その他the resultant was recrystallized in ethanol
  8. 8
    その他to obtain the white product (XII-1)

実験手順

10.0 g of 4-hydroxybenzaldehyde and 8.3 g of 1,3-dibromopropane were reacted for 24 hours in 6.2 g of potassium carbonate solution in 100 ml of DMF under reflux. The reaction mixture was poured into cold distilled water to obtain a precipitate. After filtration and vacuum drying the precipitate, the resultant was recrystallized in ethanol to obtain the white product (XII-1). The product yield was 76%.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05731599uspto-grants-1998_03