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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071254Generated: October 27, 2026

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

https://huagongshe.com/reaction/2071254

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 numberUS04046737
Source datasetuspto-grants-1977_09
ORD IDord-f45314fc69c34ddf9d0ac5b44c5d13a6
Source noteuspto-grants-1977_09