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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26681Generated: October 31, 2026

Ethyl-2-[2-(1,1-dimethylethyl)-4-oxo-4H-1-benzopyran-6-yl]propionate → Ethyl-2-[2,3-dihydro-2-(1,1-dimethylethyl)-4-oxo-4H-1-benzopyran-6-yl]propionate

https://huagongshe.com/reaction/26681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl-2-[2-(1,1-dimethylethyl)-4-oxo-4H-1-benzopyran-6-yl]propionateHCID 54572468—
ReactantJones' reagentHCID 131709961—
CatalystPalladiumHCID 23938—
SolventAcetoneHCID 180—
SolventEthanolHCID 702—
ProductEthyl-2-[2,3-dihydro-2-(1,1-dimethylethyl)-4-oxo-4H-1-benzopyran-6-yl]propionateHCID 54545077—

Reaction Steps

Ethyl-2-[2-(1,1-dimethylethyl)-4-oxo-4H-1-benzopyran-6-yl]propionate (6.61 g) was taken up in dry ethanol (150 ml) and hydrogenated at 85 p.s.i. with 5% palladium on carbon (0.2 g) and 5% palladium on barium sulphate (0.4 g) for a total of 48 hours. The catalyst was removed by filtration (`Hyflo` supercel) and the ethanol removed in vacuo affording an oil. The oil was taken up in acetone (50 ml) and treated with a slight excess of Jones reagent. The excess oxidant was destroyed with methanol and the reaction mixture was dissolved in water (200 ml) and extracted with ether. The combined ethereal extracts were washed with water, dilute aqueous sodium bicarbonate solution and water, dried (MgSO4) and concentrated in vacuo to give the title compound as an oil - 6 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04151179
Source datasetuspto-grants-1979_04
ORD IDord-ac8f4a81e1dd4b7caa6ee912ad10f7ca
Source noteuspto-grants-1979_04