Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287606Generated: October 25, 2026

Hydrochloric Acid → Ethyl 7-methoxy-1-benzofuran-2-carboxylate

https://huagongshe.com/reaction/2287606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantEthyl 2-(2-formyl-6-methoxyphenoxy)acetateHCID 2229635—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 7-methoxy-1-benzofuran-2-carboxylateHCID 52128419.5%

Reaction Steps

A solution of 2-ethoxycarbonylmethoxy-3-methoxybenzaldehyde (2.00 g) and potassium tert-butoxide (963 mg) in tetrahydrofuran (20 ml) was stirred for 1 hour under ice-cooling. Water was added to the reaction mixture, and the solution was neutralized with 1N hydrochloric acid and extracted with ethyl acetate. The extract was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by preparative thin layer chromatography (n-hexane:ethyl acetate=7:1, v/v) to give 2-ethoxycarbonyl-7-methoxybenzofuran (360 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06083961
Source datasetuspto-grants-2000_07
ORD IDord-6485e4f1f2034e4d889cfaa6e2475f4d
Source noteuspto-grants-2000_07