HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,8-Octanediamine, 4-(aminomethyl)- → 1,8-Bis[N-(2,4-bis[N-octyl-N-(2,2,6,6-tetramethylpiperid-4-yl)amino]-1,3,5-triazin-6-yl)amino]-4-[N-(2,4-bis[N-octyl-N-(2,2,6,6-tetramethylpiperid-4-yl)amino]-1,3,5-triazin-6-yl)aminomethyl]octane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,8-Octanediamine, 4-(aminomethyl)- | HCID 94211 | — |
| Reactant | 2-chloro-4,6-bis[N-octyl-N-(2,2,6,6-tetramethyl-4-piperidyl)amino]-1,3,5-triazine | HCID 20272135 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 1,8-Bis[N-(2,4-bis[N-octyl-N-(2,2,6,6-tetramethylpiperid-4-yl)amino]-1,3,5-triazin-6-yl)amino]-4-[N-(2,4-bis[N-octyl-N-(2,2,6,6-tetramethylpiperid-4-yl)amino]-1,3,5-triazin-6-yl)aminomethyl]octane | HCID 20272130 | — |
Reaction Steps
A solution of 28.3 g of 2-chloro-4,6-bis[N-octyl-N-(2,2,6,6-tetramethyl-4-piperidyl)amino]-1,3,5-triazine [prepared as described in Preparation 2(b)] and 1.0 g of 1,8-diamino-4-aminomethyloctane in 200 ml of xylene was refluxed for 10 hours. It was then treated as described in Example 1 to give a residue, which was purified by column chromatography through silica gel, eluted with a 20:1:1 by volume mixture of ethyl acetate, ethanol and triethylamine, to give the desired Compound No. 14, in the form of crystals melting at 55°-60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04533688 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-fc11622d210a480482bbbb75972badda |
| Source note | uspto-grants-1985_08 |