Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090807Generated: October 25, 2026

Ethyl Acetate → Ethyl 4,4,5,5,5-Pentafluoro-3-oxovalerate

https://huagongshe.com/reaction/1090807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPropanoic acid, 2,2,3,3,3-pentafluoro-, ethyl esterHCID 67928—
ReactantSodiumHCID 5360545—
SolventDiethyl EtherHCID 3283—
ProductEthyl 4,4,5,5,5-Pentafluoro-3-oxovalerateHCID 52220342.3%

Reaction Steps

Ethyl acetate (20.26 g, 0.23 mole) and sodium metal (2.3 g, 0.10 g-atom) was added to ethyl pentafluoropropionate (20.26 g, 0.23 mole) and the mixture was refluxed with stirring until sodium metal was dissolved. After sodium metal was dissolved, dry diethyl ether (100 ml) was added and the solution was further reacted under reflux overnight. After completion of the reaction, the solvent was evaporated under reduced pressure and the resulting residue was made acidic with 50 ml of 15% sulfuric acid, while it was cool. The solution was extracted with diethyl ether and the ether layer was dried with anhydrous sodium sulfate. Diethyl ether was then distilled off by distilling at atmospheric pressure using a fractionating column packed with Raschig ring and the resulting residue was further distilled under reduced pressure to give 9.90 g (42.3%) of the title compound as a colorless liquid, b.p. 77°-78° C./80 mmHg. The structure of this compound was confirmed by IR and NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05082947
Source datasetuspto-grants-1992_01
ORD IDord-a5c1c3ff810546b69ba645af3eb03ee6
Source noteuspto-grants-1992_01