HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291006Generated: October 30, 2026
Potassium Carbonate → Ethyl 3-(4-oxopiperidin-1-yl)propanoate
https://huagongshe.com/reaction/1291006
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Piperidone | HCID 33721 | — |
| Reactant | Ethyl 3-bromopropionate | HCID 68320 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 3-(4-oxopiperidin-1-yl)propanoate | HCID 11984242 | 66.1% |
Reaction Steps
4-Piperidinone (10.0 g, 73.7 mmol) and potassium carbonate (30.6 g, 221 mmol) were added to N,N-dimethylformamide (100 ml), and ethyl 3-bromopropionate (10.0 ml, 78.0 mmol) was added. The mixture was stirred at 60° C. for 4.5 hours. The reaction mixture was filtrated and the filtrate was added with a saturated aqueous sodium hydrogencarbonate solution (150 ml). The mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate. After filtration, low boiling matters were distilled away from the filtrate under reduced pressure and the residue was purified by silica gel column chromatography (chloroform/methanol=19/1) to give 9.70 g of ethyl 3-(4-oxopiperidino)propionate as a pale-yellow oil (66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05753670 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-0dee50a359d048319089957e1576c9cd |
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| Source note | uspto-grants-1998_05 |
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