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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80293Generated: October 24, 2026

Hydrochloric Acid → 2-(Ethoxycarbonyl)butanoic acid

https://huagongshe.com/en/reaction/80293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantDiethyl ethylmalonateHCID 8610—
ReactantPotassium HydroxideHCID 14797—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product2-(Ethoxycarbonyl)butanoic acidHCID 10898979—

Reaction Steps

Diethyl ethylmalonate was stirred overnight with 95% ethanol in the presence of 1M KOH. The white precipitate that forms was filtered out of solution, and the filtrate was concentrated under reduced pressure (e.g., on a rotary evaporator). The yellowish oil obtained upon concentration of the filtrate was added to the precipitate and the mixture was dissolved in a minimum amount of water. After acidification with dilute aqueous HCl to a pH of 2, an oil separates from the solution. The oil was taken up into diethyl ether and the aqueous layer was extracted three times with further with diethyl ether. The ether extracts were combined, dried over magnesium sulfate and filtered. A quantitative yield of 2-carboethoxybutyric acid was obtained as a yellowish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846021B2
Source datasetuspto-grants-2014_09
ORD IDord-5eb28bacb9664f2fa52b58188a0537d2
Source noteuspto-grants-2014_09