Reaktion #833515

ord-495f487bedfe4f41ae76334d5dcc0546

Reaktionsgleichung

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

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturAfter cooling
  2. 2
    Filtrationthe solid was filtered off
  3. 3
    Waschenwashed with acetone
  4. 4
    EinengenAfter complete concentration of the organic phase
  5. 5
    Sonstigethere was obtained an oily residue that
  6. 6
    Sonstigewas used directly in the second step without further purification

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07393367B2uspto-grants-2008_07