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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-tert-butyl 2-ethyl 5-oxohexahydropentalene-2,2(1H)-dicarboxylate | HCID 86690104 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 5-oxooctahydropentalene-2-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09326973B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-2775b74e14354afda0777932d703f284 |
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| Source note | uspto-grants-2016_05 |
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