HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132765Generated: October 30, 2026
Iodoethane → Ethyl 1-ethyl-2-oxocyclopentane-1-carboxylate
https://huagongshe.com/reaction/132765
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-oxocyclopentanecarboxylate | HCID 69136 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 1-ethyl-2-oxocyclopentane-1-carboxylate | HCID 10607544 | 96.7% |
Reaction Steps
Under vigorously agitation, 31.2 g (purity of 90%,) of ethyl 2-oxocyclopentane carboxylate was added to 76.04 g (purity of 98%) of ground anhydrous potassium carbonate, and after stirring for several minutes, to the mixture was added 100 ml of acetone. The reaction mixture was further stirred for about 15 minutes, then to the mixture was dropwise added 29.51 ml (purity of 98.5%) of ethyl iodide. Upon the completion of the addition, the reaction mixture was heated for reflux for 5 hours. The reaction mixture was filtered under the reduced pressure, and the filter cake was washed with diethyl ether until its color was purely white. Pale yellow filtrate was collected and dried over anhydrous magnesium sulfate, then the solvent was removed. The residue was distilled under reduced pressure, and 32.03 g of colorless liquid as a distillate cut of 130-134° C./18 mmHg was collected. Yield-96.7%. MS: m/e 184(M+′), 156(M+″—C2H5), 140(M+′—OCH2CH3), 139, 101(M+′—CO2CH2CH3), 127(155—CH2CH2), 111(156-OCH2CH3), 55(base).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07388103B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-68854d3d137a41be83c56691eb7f58a5 |
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| Source note | uspto-grants-2008_06 |
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