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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063340Generated: October 31, 2026

Hydrochloric Acid → Ethyl 3-oxo-3-(pyrimidin-4-yl)propanoate

https://huagongshe.com/reaction/2063340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl pyrimidine-4-carboxylateHCID 13639438—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductEthyl 3-oxo-3-(pyrimidin-4-yl)propanoateHCID 1196145892%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of ethanol (16.18 g, 0.351 mol) in diethyl ether (15 ml) was added to a solution of sodium hydride (13.71 g, 0.343 mol, 60% in paraffin, paraffin was removed by washing with hexane) in diethyl ether (100 ml). After stirring the mixture for 30 minutes, the solvent was evaporated under reduced pressure, and toluene (100 ml) was added to the residue. The solution was added with a solution of ethyl pyrimidine-4-carboxylate (intermediate 5, 30.86 g, 0.203 mol) and ethyl acetate (30.48 g, 0.346 mol) in toluene (100 ml), and the mixture was heated at 80° C. for 3 hours. The mixture was added with hydrochloric acid and then sodium bicarbonate to be adjusted to pH 4. The solution was partitioned between water and ethyl acetate. The organic layer was washed with brine and dried over sodium sulfate. The solvent was evaporated under reduced pressure to give ethyl 3-oxo-3-(pyrimidin-4-yl)propionate (intermediate 6, 36.10 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288383B2
Source datasetuspto-grants-2012_10
ORD IDord-4e64f84356544c568c2593fc7e818f42
Source noteuspto-grants-2012_10