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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Trans-4-(2-oxo-pyrrolidin-1-yl)cyclohexanecarboxylic acid | HCID 11572026 | — |
| Product | Ethyl 4-(2-oxopyrrolidin-1-yl)cyclohexane-1-carboxylate | HCID 23115699 | 102% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07439368B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-e09600a75ac148709deffda14bde2324 |
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| Source note | uspto-grants-2008_10 |
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