HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,6,6-Tetramethyl-4-piperidone → 1,6-Bis(2,2,6,6-tetramethyl-4-piperidylamino)hexane
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 | 90.1% |
Reaction Steps
In a 5 liter autoclave were charged 981 g (6.32 mols) of 2,2,6,6-tetramethyl-4-piperidone, 350 g (3.01 mols) of hexamethylenediamine, 1500 g of methanol and 5.0 g of 5% platinum on carbon with keeping the temperature at 45°-55° C. The inside of the autoclave was pressurized to 40 bars with hydrogen and heated to 70°-80° C. to carry out hydrogenation. The hydrogenation was completed after 4-5 hours. The catalyst was removed by filtration at 70°-80° C. under 2-3 bars and 1070 g of N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine was obtained by distillation. Yield: 90%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05478873 |
| Source dataset | uspto-grants-1995_12 |
| ORD ID | ord-4a04102d9e094b87b2ae59decae3f020 |
| Source note | uspto-grants-1995_12 |