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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49458Generated: October 25, 2026

Hydrochloric Acid → Ethyl 7-amino-4-oxo-4H-chromene-2-carboxylate

https://huagongshe.com/reaction/49458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl OxalateHCID 7268—
ReactantSodium ethoxideHCID 2723922—
ReactantN-(4-acetyl-3-hydroxyphenyl)acetamideHCID 2775185—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductEthyl 7-amino-4-oxo-4H-chromene-2-carboxylateHCID 1072832561%

Reaction Steps

A solution of N-(4-acetyl-3-hydroxyphenyl)acetamide (4.00 g., 21 mmol) and diethyl oxalate (7.3 mL, 54 mmol) in absolute ethanol is added dropwise to a solution of sodium ethoxide (0.1 mol) in absolute ethanol. The mixture is heated at reflux temperature for 1.5 h, cooled to ambient temperature, poured into water, acidified to pH 3 with 6N HCl and extracted with ethyl acetate. The extracts are combined and concentrated in vacuo to afford an oily residue. The residue is dissolved in ethanol, treated with concentrated HCl heated at reflux temperature overnight, cooled to 0° C. for several hours and filtered. The filtercake is dried to afford the title compound as an orange solid, 2.95 g (61% yield), mp 195°-198° C., identified by NMR and mass spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706757B2
Source datasetuspto-grants-2004_03
ORD IDord-dc86013d85064869934468b248415d6a
Source noteuspto-grants-2004_03