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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-oxocyclopentanecarboxylateHCID 69136—
SolventAcetoneHCID 180—
ProductEthyl 1-ethyl-2-oxocyclopentane-1-carboxylateHCID 1060754496.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388103B2
Source datasetuspto-grants-2008_06
ORD IDord-68854d3d137a41be83c56691eb7f58a5
Source noteuspto-grants-2008_06