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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520391Generated: October 25, 2026

Trifluoroacetic acid → Ethyl 5-oxooctahydropentalene-2-carboxylate

https://huagongshe.com/reaction/520391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-tert-butyl 2-ethyl 5-oxohexahydropentalene-2,2(1H)-dicarboxylateHCID 86690104—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-oxooctahydropentalene-2-carboxylateHCID 73030532—

Reaction Steps

To a solution of 2-tert-butyl 2-ethyl 5-oxohexahydropentalene-2,2(1H)-dicarboxylate (0.8 g, 2.70 mmol) in DCM (4 mL) was added TFA (2.080 mL) and the reaction mixture was stirred at rt for 4 h. The reaction mixture was evaporated to dryness and the residue was dissolved in pyridine (5 mL) and heated to reflux for 4 h until decarboxylation was complete. Pyridine was evaporated and the residue was purified by silica gel chromatography (10% EtOAC in DCM) to afford ethyl 5-oxooctahydropentalene-2-carboxylate (a mixture of endo/exo isomers) as a clear oil. 1H NMR (500 MHz, CDCl3) δ ppm 4.10-4.18 (2H, m), 2.85-3.02 (2H, m), 2.69-2.80 (1H, m), 2.44-2.56 (2H, m), 2.20-2.36 (2H, m), 2.10-2.20 (1H, m), 2.04 (1H, dd, J=19.45, 4.65 Hz), 1.66-1.80 (2H, m), 1.22-1.31 (3H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09326973B2
Source datasetuspto-grants-2016_05
ORD IDord-2775b74e14354afda0777932d703f284
Source noteuspto-grants-2016_05