HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090409Generated: October 30, 2026
Ethyl 4-oxo-1-piperidinecarboxylate → HCID 14770818, compound
https://huagongshe.com/reaction/1090409
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 4-oxo-1-piperidinecarboxylate | HCID 34767 | — |
| Reactant | 1,4-Dibromo-2,5-difluorobenzene | HCID 67596 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 14770818 | HCID 14770818 | — |
Reaction Steps
A solution of 16.55 g (60.85 mmol) 1,4-dibromo-2,5-difluorobenzene in 400 ml of ethyl ether stirred at -75° C. under an argon atmosphere was treated dropwise with 24.3 ml of 2.5 M n-butyl lithium in hexane. The mixture was let warm to -50° C. and treated dropwise with a solution of 11.00 g (64.33 mmol) 1-ethoxycarbonyl-4-piperidone in 100 ml ethyl ether. After stirring a further 0.25 hour, the mixture was let warm to room temperature and extracted with ammonium chloride solution. The organic layer was dried (MgSO4), evaporated and the crude product chromatographed on a silica gel column and crystallized from toluene hexane to afford the title compound, mp 133°-136° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05081254 |
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| Source dataset | uspto-grants-1992_01 |
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| ORD ID | ord-e3305e39836043779a4c8bdea71f1ec0 |
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| Source note | uspto-grants-1992_01 |
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