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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116764Generated: October 30, 2026

Ethanol → Ethyl 4-(2-oxopyrrolidin-1-yl)cyclohexane-1-carboxylate

https://huagongshe.com/reaction/2116764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSulfuric AcidHCID 1118—
ReactantSodium BicarbonateHCID 516892—
ReactantTrans-4-(2-oxo-pyrrolidin-1-yl)cyclohexanecarboxylic acidHCID 11572026—
ProductEthyl 4-(2-oxopyrrolidin-1-yl)cyclohexane-1-carboxylateHCID 23115699102%

Reaction Conditions

Temperature10 °C

Reaction Steps

To 4-(2-pyrrolidon-1-yl)cyclohexylcarboxylic acid are added ethanol (30 mL, 10V/W) and conc. sulfuric acid (0.4 g, 0.2 W/W), and the mixture is heated to reflux for 3.5 hours. After cooling the reaction solution to 10° C., sodium bicarbonate (powder) is thereto added. After foaming is stopped, ethanol is evaporated under reduced pressure. The residue is extracted with ethyl acetate and saturated brine. The resultant solution is dried over magnesium sulfate and evaporated to remove the solvent under reduced pressure to give ethyl 4-(2-pyrrolidon-1-yl)cyclohexylcarboxylate (oil, 2.3 g, 102%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439368B2
Source datasetuspto-grants-2008_10
ORD IDord-e09600a75ac148709deffda14bde2324
Source noteuspto-grants-2008_10