Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | 2,6-Diethyl-2,3,6-trimethylpiperidin-4-one | HCID 22182213 | — |
| Catalyst | HCID 178503042 | HCID 178503042 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 20348257 | HCID 20348257 | — |
Reaction Steps
197.3 g of 2,6-diethyl-2,3,6-trimethylpiperidine-4-one and 30.0 g of ethylenediamine are dissolved in one liter of methanol. 10 g of a platin-carbon catalyst (5% b.w. Pt) are added, and the solution is hydrogenated at 30°-35° C. and normal pressure. Hydrogenation is completed after 106 hours. The catalyst is filtered off, the solvent is evaporated in vacuo, and the oily residue is purified by molecular distillation at 150° C. and 0.005 mm Hg. N,N'-Bis-(2,6-diethyl-2,3,6-trimethyl-4-piperidyl)-ethylenediamine (compound no. 7) is obtained as a practically colourless oil. If, instead of 30.0 g of ethylenediamine an equivalent amount of 1,6-hexamethylenediamine is used and otherwise the procedure described above is followed, after molecular distillation at 180° C. and 0.002 mm Hg. N,N'-Bis-(2,6-diethyl-2,3,6-trimethyl-4-piperidyl)-hexamethylene-1,6-diamine (compound no. 8) is obtained in the form of a thick colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04191683 |
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| Source dataset | uspto-grants-1980_03 |
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| ORD ID | ord-29982e95c6664487915f8a630bb1267e |
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| Source note | uspto-grants-1980_03 |
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