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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603869Generated: October 30, 2026

Ethyl 4-oxo-4H-1-benzopyran-2-carboxylate → Ethyl Chroman-2-carboxylate

https://huagongshe.com/reaction/1603869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-oxo-4H-1-benzopyran-2-carboxylateHCID 26861—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductEthyl Chroman-2-carboxylateHCID 1290909484%

Reaction Steps

A solution of ethyl 4-oxo-4H-1-benzopyran-2-carboxylate (2.0 g, 9.17 mmol) in methanol (60 ml), chloroform (25 ml) and glacial acetic acid (20 ml) was added with 10% palladium-on-charcoal and the mixture was left under stirring at room pressure and temperature for 24 h. under hydrogen atmosphere. After that, the catalyst was filtered off and the filtrate was evaporated to dryness. The residue was redissolved in ethyl ether and washed successively with a 5% sodium bicarbonate solution and a sodium chloride saturated solution. The mixture was dried and the solvent was evaporated off under reduced pressure, to obtain 1.575 g of the title product (84% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990142
Source datasetuspto-grants-1999_11
ORD IDord-0493502a233544249da36db96ee3a3b0
Source noteuspto-grants-1999_11