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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 126844Generated: October 26, 2026

Formaldehyde → 2-(4-Carboxy-1-piperidylmethyl)propenenitrile

https://huagongshe.com/reaction/126844

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 numberUS04254131
Source datasetuspto-grants-1981_03
ORD IDord-795c2fe996f04679b20f677fffa08308
Source noteuspto-grants-1981_03