Réaction #1328425

ord-169f1178365149fb86f98932f7f04ab5

Équation de réaction

Cl
hydrochloric acid
C=CCBr
allyl bromide
[K+].[OH-]
potassium hydroxide
COC(=O)c1ccc(OC)c(C=O)c1O
methyl 2-hydroxy-3-formyl-4-methoxybenzoate
C=CCOc1c(C(=O)OC)ccc(OC)c1C=O
methyl 2-allyloxy-3-formyl-4-methoxybenzoate
Rendement 36.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionextracted with ethyl acetate
  2. 2
    LavageThe combined organic phases were washed with water
  3. 3
    Autredried
  4. 4
    Autrethe solvent was removed

Mode opératoire

At room temperature, 23.2 g (0.192 mol) of allyl bromide were added dropwise to a mixture of 21.0 g (0.375 mol) of potassium hydroxide and 20.2 g (0.096 mol) of methyl 2-hydroxy-3-formyl-4-methoxybenzoate in 500 ml of dimethyl sulfoxide, and the mixture was stirred at room temperature for 4 hours. The mixture was subsequently stirred into 1.5 l of 3% strength aqueous hydrochloric acid and extracted with ethyl acetate. The combined organic phases were washed with water and dried, and the solvent was removed. Silica gel chromatography using cyclohexane/ethyl acetate=1:2 gave 7.7 g (36%) of methyl 2-allyloxy-3-formyl-4-methoxybenzoate in the form of a yellowish oil.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07115545B1uspto-grants-2006_10