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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922439Generated: October 29, 2026

Hydrochloric Acid → Ethyl 4-hydroxybenzofuran-6-carboxylate

https://huagongshe.com/reaction/922439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Benzofurancarboxylic acid, 4-(acetyloxy)-, ethyl esterHCID 67545162—
SolventEthanolHCID 702—
ProductEthyl 4-hydroxybenzofuran-6-carboxylateHCID 1134475795.5%

Reaction Steps

To a solution of the compound obtained in the above (1) (24.7 g) in ethanol (150 mL) was added potassium carbonate (42.0 g), and the mixture was heated to reflux for 30 minutes. The reaction mixture was ice-cooled, and then acidified by 10% hydrochloric acid, and then extracted with ethyl acetate. The organic layer was washed with saturated saline, dried over sodium sulfate, and then concentrated under reduced pressure. The resulting residue was triturated with n-hexane-dichloromethane (5:1) to give ethyl 4-hydroxy-1-benzofuran-6-carboxylate [REx(7-1)] (19.6 g) as a pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278944B2
Source datasetuspto-grants-2016_03
ORD IDord-3593af004da64766a74ae4905e6e0957
Source noteuspto-grants-2016_03