Reacción #833515

ord-495f487bedfe4f41ae76334d5dcc0546

Ecuación de reacción

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

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaAfter cooling
  2. 2
    Filtraciónthe solid was filtered off
  3. 3
    Lavadowashed with acetone
  4. 4
    ConcentraciónAfter complete concentration of the organic phase
  5. 5
    Otrothere was obtained an oily residue that
  6. 6
    Otrowas used directly in the second step without further purification

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07393367B2uspto-grants-2008_07