Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241243Generated: October 25, 2026

Hydrochloric Acid → Methyl 2-allyloxy-3-formyl-4-methoxybenzoate

https://huagongshe.com/reaction/1241243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAllyl bromideHCID 7841—
ReactantPotassium HydroxideHCID 14797—
Reactant3-Formyl-2-hydroxy-4-methoxy-benzoic acid methyl esterHCID 21933599—
SolventDimethyl SulfoxideHCID 679—
ProductMethyl 2-allyloxy-3-formyl-4-methoxybenzoateHCID 2193358736%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115545B1
Source datasetuspto-grants-2006_10
ORD IDord-169f1178365149fb86f98932f7f04ab5
Source noteuspto-grants-2006_10