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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484945Generated: October 30, 2026

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

https://huagongshe.com/reaction/484945

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Octanediamine, 4-(aminomethyl)-HCID 94211—
Reactant2-chloro-4,6-bis[N-octyl-N-(2,2,6,6-tetramethyl-4-piperidyl)amino]-1,3,5-triazineHCID 20272135—
SolventO-XyleneHCID 7237—
Product1,8-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]octaneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04533688
Source datasetuspto-grants-1985_08
ORD IDord-fc11622d210a480482bbbb75972badda
Source noteuspto-grants-1985_08