HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66649Generated: October 26, 2026
Carbon Dioxide → 2-(4-Fluoro-1-piperidylmethyl)propenenitrile
https://huagongshe.com/reaction/66649
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Fluoropiperidine | HCID 2759159 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(4-Fluoro-1-piperidylmethyl)propenenitrile | HCID 13041034 | — |
Reaction Steps
4-Fluoropiperidine (0.7 g., 0.005 mole) was dissolved in a mixture of 3 ml. of dioxane and 2 ml. of water containing cyanoacetic acid (0.43 g., 0.005 mole). The solution was heated to 65° C. and carbon dioxide evolution began. It was maintained at 60°-65° C. for 21/2 hours and allowed to stand overnight. A solid gummy residue, 1 gm., was obtained upon stripping in a bath at 55° C. and at 1 mm. It was taken up in a small amount of water, made alkaline with sodium bicarbonate and extracted with ether. The organic layer was water washed and dried over anhydrous sodium sulfate. After solvent stripping, the product was obtained as a colorless oil, 0.7 g., of analytical purity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04342872 |
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| Source dataset | uspto-grants-1982_08 |
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| ORD ID | ord-74e54ba5eb154ef3b5f40bb5afe8d738 |
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| Source note | uspto-grants-1982_08 |
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