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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390113Generated: October 28, 2026

Carbon Dioxide → 2-Methylpiperidine

https://huagongshe.com/reaction/1390113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantFormaldehydeHCID 712—
ReactantCyanoacetic acidHCID 9740—
ReactantPiperidine, 4-(1,1-dimethylethyl)-HCID 74661—
Reactant2-[(2-Methyl-1-piperidyl)methyl]propenenitrileHCID 54220988—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product2-MethylpiperidineHCID 7974—
ProductPiperidine, 4-(1,1-dimethylethyl)-HCID 74661—

Reaction Steps

Cyanoacetic acid (1.75 g., 0.02 mole) was dissolved in 10 ml. of dioxane. In a five minute period 4-t-butylpiperidine (2.8 g., 0.02 mole) was added, the temperature rose to 25° C. from 15° C. obtained by prior cooling with an ice bath. The mixture which solidified became fluid upon the addition of 37% aqueous formaldehyde (3.6 g., 0.04 mole), the temperature rose to 30° C. and carbon dioxide evolution began. The mixture was stirred an additional 12 hours, was taken up in ether and the organic phase separated and washed with water. The dried ether solution was stripped to solvent to leave a solid residue product, 3.7 g. of practically analytical purity. In place of 4-t-butylpiperidine, the use of 2-methylpiperidine (0.02 mole) provided 2-[(2-methyl-1-piperidyl)methyl]propenenitrile as a colorless oil, RfSiO2 0.58 (5% ethanol in methylene chloride).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04247700
Source datasetuspto-grants-1981_01
ORD IDord-6c53b34cd71541d8a4b5d2626621cab7
Source noteuspto-grants-1981_01