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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978768Generated: October 29, 2026

Hydrochloric Acid → 6-Methoxy-1-benzofuran-2-carboxylic acid

https://huagongshe.com/reaction/1978768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Hydroxy-4-MethoxybenzaldehydeHCID 69600—
ReactantDiethyl bromomalonateHCID 69637—
SolventWaterHCID 962—
Product6-Methoxy-1-benzofuran-2-carboxylic acidHCID 91886346.7%

Reaction Steps

To a suspension of 2-hydroxy-4-methoxybenzaldehyde (20.0 g) and potassium carbonate (20.0 g) in2-butanone (80 ml) was added diethyl bromomalonate (39.3 g), and the mixture was refluxed under nitrogen atmosphere for 7 hours and cooled. To the mixture was added water, and the mixture was made acidic with 1N hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried with magnesium sulfate. Under reduced pressure, the solvent was evaporated, and the resulting dark brown oil was suspended in a solution of potassium hydroxide (20.0 g) in ethanol (200 ml). The suspension was refluxed for 1 hour and cooled, and to the mixture was added water. The mixture was made acidic with 1N hydrochloric acid and extracted with ethylacetate(twice). The organic layer was washed with water and saturated brine, and dried with magnesium sulfate. Under reduced pressure, the solvent was evaporated, and the resulting solid was washed with hexane to give yellow solid of 6-methoxybenzofuran-2-carboxylic acid (11.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235771B1
Source datasetuspto-grants-2001_05
ORD IDord-79f5bae4553c4b91b1499b809ee56d04
Source noteuspto-grants-2001_05