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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 126839Generated: October 25, 2026

Carbon Dioxide → 2-[(4-t-Butyl-1-piperidyl)methyl]propenenitrile

https://huagongshe.com/reaction/126839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantFormaldehydeHCID 712—
ReactantCyanoacetic acidHCID 9740—
ReactantPiperidine, 4-(1,1-dimethylethyl)-HCID 74661—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
Product2-[(4-t-Butyl-1-piperidyl)methyl]propenenitrileHCID 13041035—

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 of solvent to leave a solid residue product, 3.7 g. of practically analytical purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04254131
Source datasetuspto-grants-1981_03
ORD IDord-bcafefd463434a369923d6a6c2a36c1a
Source noteuspto-grants-1981_03