Reacción #1985940

ord-120dc1751cde4571b1c1a8542de45155

Ecuación de reacción

COc1cc(C=O)ccc1O
vanillin
CCN(CC)CC
triethylamine
CC(=O)OC(C)=O
acetic anhydride
COc1cc(C=O)ccc1OC(C)=O
desired product
COc1cc(C=O)ccc1OC(C)=O
4-Acetoxy-3-methoxybenzaldehyde

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Lavadothe solution washed with water, brine
  2. 2
    Secadodried over magnesium sulfate
  3. 3
    Filtraciónfiltered
  4. 4
    Concentraciónconcentrated in vacuo

Procedimiento

A solution of vanillin (60.8 g), triethylamine (60 ml), acetic anhydride (44 ml), and 4-dimethylaminopyridine (1.0 g) in methylene chloride (800 ml) is stirred at room temperature for about 30 minues, and the volume then reduced by 50% in vacuo. The residue is diluted with ether and the solution washed with water, brine, dried over magnesium sulfate, filtered and concentrated in vacuo to give the desired product.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05571506uspto-grants-1996_11