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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547498Generated: November 2, 2026

Ethanol → Ethyl 2-oxooctahydropentalene-3a-carboxylate

https://huagongshe.com/reaction/547498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHCID 57686983HCID 57686983—
CatalystPalladiumHCID 23938—
ProductEthyl 2-oxooctahydropentalene-3a-carboxylateHCID 1097640481%

Reaction Steps

Methyl 5-oxo-1,2,3,3a,4,5-hexahydropentalene-3a-carboxylate (2.5 g, 12.8 mmol) in ethanol (25 mL) was purged with nitrogen for about 10 minutes with stirring. Palladium on carbon (0.043 g, 20 mol %) was added and the reaction vessel was purged with nitrogen for about 10 minutes. The flow of nitrogen was stopped and the flask was flushed with hydrogen. The reaction mixture was stirred overnight under an atmosphere of hydrogen. The flask was flushed with nitrogen for about 20 minutes. The reaction mixture was passed through a pad of Celite® and the filtrate was concentrated in vacuo. The residue was purified by flash column chromatography (eluting with 25% ethyl acetate/heptane) to afford ethyl 2-oxooctahydropentalene-3a-carboxylate (2.04 g, 10.4 mmol, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939544B2
Source datasetuspto-grants-2011_05
ORD IDord-e7fe4ac3471d449894f4a5ffe8b66b27
Source noteuspto-grants-2011_05