Реакция #833515

ord-495f487bedfe4f41ae76334d5dcc0546

Уравнение реакции

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

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураAfter cooling
  2. 2
    Фильтрацияthe solid was filtered off
  3. 3
    Промывкаwashed with acetone
  4. 4
    КонцентрированиеAfter complete concentration of the organic phase
  5. 5
    Другоеthere was obtained an oily residue that
  6. 6
    Другоеwas used directly in the second step without further purification

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07393367B2uspto-grants-2008_07