HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 126865Generated: October 30, 2026
Tetrahydrofuran → HCID 20288021, compound
https://huagongshe.com/reaction/126865
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 4-oxo-1-piperidinecarboxylate | HCID 34767 | — |
| Reactant | HCID 53666596 | HCID 53666596 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20288021 | HCID 20288021 | 83% |
Reaction Steps
To a stirred mixture of 41 parts of diethyl [2-(3-methoxyphenyl)-2-oxoethyl]phosphonate and 180 parts of tetrahydrofuran are added portionwise 5 parts of sodium hydride dispersion 61% while cooling at about 15° C. Upon completion, stirring is continued for 30 minutes at room temperature. Then there are added dropwise 21 parts of ethyl 4-oxo-1-piperidinecarboxylate at about 20° C. Stirring is continued for 4 hours at 60° C. The reaction mixture is cooled, water is added and the layers are separated. The organic phase is dried, filtered and evaporated. The residue is distilled, yielding 30 parts (83%) of ethyl 2,3-dihydro-4-[2-(3-methoxyphenyl)-2-oxoethyl]-1(6H)-pyridinecarboxylate; bp. 200°-210° C. at 1 mm. pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04254127 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-9a91ce810a6f4335986020b65d21134f |
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| Source note | uspto-grants-1981_03 |
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