HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 126837Erstellt: 25. Oktober 2026
Carbon Dioxide → 2-(4-Fluoro-1-piperidylmethyl)propenenitrile
https://huagongshe.com/reaction/126837
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Carbon Dioxide | HCID 280 | — |
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | Cyanoacetic acid | HCID 9740 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 4-Fluoropiperidine | HCID 2759159 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 2-(4-Fluoro-1-piperidylmethyl)propenenitrile | HCID 13041034 | — |
Reaktionsschritte
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). Then, 0.85 g. (0.01 mole) of 37% aqueous formaldehyde was added to the solution. 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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04254131 |
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| Quelldatensatz | uspto-grants-1981_03 |
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| ORD ID | ord-bbf5626a65f8497384b49ee61d97e8ac |
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| Quellennotiz | uspto-grants-1981_03 |
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