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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434442Generated: October 27, 2026

Acrylonitrile → 4-(2'-Cyanoethoxy) 1,2,2,6,6-pentamethylpiperidine

https://huagongshe.com/reaction/434442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylonitrileHCID 7855—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Piperidinol, 1,2,2,6,6-pentamethyl-HCID 75472—
SolventBenzeneHCID 241—
Product4-(2'-Cyanoethoxy) 1,2,2,6,6-pentamethylpiperidineHCID 20492358—

Reaction Steps

2.65 parts of acrylonitrile was added dropwise with stirring to a solution of 8.55 parts of 1,2,2,6,6-pentamethylpiperidin-4-ol and 0.30 parts of 40% potassium hydroxide solution in 80 parts of benzene. Stirring was continued at room temperature for 16 hours after which time the solution was washed with water, dried and the benzene solvent removed by distillation under reduced pressure. Fractional distillation of the residue, under reduced pressure gave 1.70 parts of 4-(2'-cyanoethoxy)-1,2,2,6,6-pentamethylpiperidine having a boiling point of 105°-6° C. at 0.1 mm of Hg and the following elemental analysis by weight:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE031342
Source datasetuspto-grants-1983_08
ORD IDord-314c2ff11d4143bda105ae4ec5cf6605
Source noteuspto-grants-1983_08