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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49459Generated: October 28, 2026

Ethyl 7-amino-4-oxo-4H-chromene-2-carboxylate → Ethyl 7-Amino-2-chromancarboxylate

https://huagongshe.com/reaction/49459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 7-amino-4-oxo-4H-chromene-2-carboxylateHCID 10728325—
CatalystPalladiumHCID 23938—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductEthyl 7-Amino-2-chromancarboxylateHCID 1063277489%

Reaction Steps

A solution of ethyl 7-amino-4-oxo-4H-chromene-2-carboxylate (1.00 g, 4.3 mmol) in ethanol and concentrated HCl (5 mL) is hydrogenated over 10% Pd/C (0.5 g) at 50 psi for 72 h at ambient temperature. The reaction mixture is filtered and the filtrate is concentrated in vacuo. The resultant residue is dissolved in ethyl acetate and washed with saturated aqueous NaHCO3. The organic phase is dried over MgSO4, and concentrated in vacuo to afford the title compound as an amber oil, 0.85 g (89% yield), identified by NMR and mass spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706757B2
Source datasetuspto-grants-2004_03
ORD IDord-e2da5b6fc92c4373bfb43f28abe30963
Source noteuspto-grants-2004_03