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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109796Generated: October 31, 2026

2,2,6,6-Tetramethyl-4-piperidone → 1,6-Bis(2,2,6,6-tetramethyl-4-piperidylamino)hexane

https://huagongshe.com/reaction/1109796

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,6,6-Tetramethyl-4-piperidoneHCID 13220—
ReactantHexamethylenediamineHCID 16402—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventMethanolHCID 887—
Product1,6-Bis(2,2,6,6-tetramethyl-4-piperidylamino)hexaneHCID 93419—

Reaction Steps

After 1,047 parts of 2,2,6,6-tetramethyl-4-piperidone, 373 parts of hexamethylenediamine, 2,260 parts of methanol and 5.5 parts of 5% platinum-on-carbon catalyst were charged into an autoclave, the temperature of the mixture was gradually elevated from 30° C. and the mixture was subjected to hydrogenation at a hydrogen pressure of 5 kg/cm2 while the temperature was kept at 60°-70° C. It took 8 hours to complete the hydrogenation. The resultant mixture was filtered at about 50°-60° C. to remove the catalyst therefrom, and then the resultant filtrate was subjected to distillation to remove the solvent and the water formed as by-product during the reaction, thereby obtaining 1,325 parts of crude N,N'-bis (2,2,6,6-tetramethyl-4-piperidyl)hexamethylenediamine having a purity of 92.9%, a 2,2,6,6-tetramethyl-4-piperidone content of 0.8%, and an APHA value of 400.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05322947
Source datasetuspto-grants-1994_06
ORD IDord-e1b9934b226043e9ba0994052041dd5b
Source noteuspto-grants-1994_06