HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 993055Generated: November 1, 2026
Tetrahydrofuran → Ethyl 2-(piperidin-4-ylidene)acetate
https://huagongshe.com/reaction/993055
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Piperonylamine | HCID 2723901 | — |
| Product | Ethyl 2-(piperidin-4-ylidene)acetate | HCID 18695502 | — |
Reaction Steps
To a suspension of sodium hydride (2.6 g) in 30 ml of tetrahydrofuran, cooled to 0° C. and kept under nitrogen atmosphere, 13 ml of triethylphosphonoacetate, dissolved in 10 ml of tetrahydrofuran are added dropwise. The temperature is then brought to room temperature and the stirring is continued for 30 minutes. The mixture is again cooled to 0° C. and it is added dropwise with a solution obtained by adding portionwise to a solution of 4-piperidone monohydrate hydrochloride (10 g) in THF 2.6 g of sodium hydride, filtered to eliminate the sodium chloride which formed. At the end of the addition, the temperature is brought to room temperature and the stirring is continued for 20 hours. The solvent is then evaporated under reduced pressure and the residue is redissolved in ethyl acetate and washed with 1 N hydrochloric acid. The aqueous phase is extracted with ethyl acetate and chloroform, then it is basified to pH=9-10 by adding 20% sodium hydroxide and it is extractedb with chloroform. The aqueous phase is then salted and extracted again with chloroform three times. The pooled extracts are dried over sodium sulfate and evaporated to give 7.1 g of the product as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06472396B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-7a3ebf7202f34d7dab3f84090aea74c0 |
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| Source note | uspto-grants-2002_10 |
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