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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258783Generated: October 30, 2026

Acrylonitrile → HCID 21425715, compound

https://huagongshe.com/reaction/258783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylonitrileHCID 7855—
Reactant3-Piperidin-3-yl-propylamineHCID 12247576—
ReactantHCID 21425721HCID 21425721—
ProductHCID 21425715HCID 21425715—

Reaction Steps

For example, 3-(3-aminopropyl)piperidine may be converted to a Schiff base with 1,5-di-(3-isopropylnorborn-2-yl)-3-pentanone, catalytically reduced, then the resulting amine selectively cyanoethylated on the ring nitrogen with acrylonitrile, followed by catalytic hydrogenation to furnish 1-(3-aminopropyl)-3-{3-[1,5-di-(3-isopropylnorborn-2-yl)-3-pentylamino]propyl}piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04033748
Source datasetuspto-grants-1977_07
ORD IDord-8605dac52ee444388423bc96e9f1aabd
Source noteuspto-grants-1977_07