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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2,6,6-Tetramethyl-4-piperidone | HCID 13220 | — |
| Reactant | Hexamethylenediamine | HCID 16402 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1,6-Bis(2,2,6,6-tetramethyl-4-piperidylamino)hexane | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05322947 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-e1b9934b226043e9ba0994052041dd5b |
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| Source note | uspto-grants-1994_06 |
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