HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,2,2,6,6-Pentamethylpiperidin-4-amine → 2-Hydroxy-1,3-bis[N-methyl-N-(2,2,6,6-tetramethyl-4-piperidyl)amino]propane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,2,2,6,6-Pentamethylpiperidin-4-amine | HCID 13657792 | — |
| Reactant | 4-[N-(2,3-epoxypropyl)-N-methylamino]-2,2,6,6-tetramethylpiperidine | HCID 20393554 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Hydroxy-1,3-bis[N-methyl-N-(2,2,6,6-tetramethyl-4-piperidyl)amino]propane | HCID 20393553 | — |
Reaction Steps
A mixture of 2.2 g of 4-[N-(2,3-epoxypropyl)-N-methylamino]-2,2,6,6-tetramethylpiperidine and 1.7 g of 4-methylamino-2,2,6,6-tetramethylpiperidine in 20 ml of benzene was refluxed, with stirring, for 3 hours. At the end of this time, the solvent was removed from the reaction mixture by evaporation under reduced pressure and then the resulting residue was distilled in vacuo, giving the desired compound in the form of a colourless, viscous oil boiling at 194°-196° C. at 0.2 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04166813 |
| Source dataset | uspto-grants-1979_09 |
| ORD ID | ord-f27e607aba4d464f8a53aa12032fb160 |
| Source note | uspto-grants-1979_09 |