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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant4-Piperidinecarboxylic acidHCID 3773—
ReactantSodium ChlorideHCID 5234—
ReactantCyanoacetic acidHCID 9740—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product2-(4-Carboxy-1-piperidylmethyl)propenenitrileHCID 13037608—

Reaction Conditions

Temperature35 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04342872
Source datasetuspto-grants-1982_08
ORD IDord-6bd5bd60a0f443a8943465267abf582a
Source noteuspto-grants-1982_08