HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66655Generated: October 23, 2026
Formaldehyde → 2-(4-Carboxy-1-piperidylmethyl)propenenitrile
https://huagongshe.com/en/reaction/66655
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 4-Piperidinecarboxylic acid | HCID 3773 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(4-Carboxy-1-piperidylmethyl)propenenitrile | HCID 13037608 | — |
Reaction Steps
Cyanoacetic acid (12.8 g. 0.15 mole) was dissolved in 25 ml. of dioxane. Next, isonipecotic acid (19.4 g., 0.15 mole) was added. Then, 37% aqueous formaldehyde (25 g., 0.3 mole) was dripped in and the temperature maintained at a maximum of 35° C. After mixing overnight sodium chloride was added to saturation and methylene chloride used to extract the mixture. The organic phase was washed with water, dried over anhydrous sodium sulfate and after filtration, concentrated. Most of the product appeared in the aqueous phase. This was extracted twice with 500 ml. of methylene chloride in a continuous extractor. The residue obtained after solvent removal weighed 14.2 g., m.p. 109°-111° C. 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-6bd5bd60a0f443a8943465267abf582a |
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| Source note | uspto-grants-1982_08 |
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