Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569194Generated: October 25, 2026

N,N'-Diallyl-6-chloro-1,3,5-triazine-2,4-diamine → 2,4-Bis-allylamino-6-[2-(2,2,6,6-tetramethylpiperid-4-yl)-ethylamino]-1,3,5-triazine

https://huagongshe.com/reaction/569194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-Diallyl-6-chloro-1,3,5-triazine-2,4-diamineHCID 27306—
Reactant4-Piperidineethanamine, 2,2,6,6-tetramethyl-HCID 12567367—
SolventO-XyleneHCID 7237—
Product2,4-Bis-allylamino-6-[2-(2,2,6,6-tetramethylpiperid-4-yl)-ethylamino]-1,3,5-triazineHCID 70415291—

Reaction Steps

18.05 g (0.08 mole) of 2,4-bis-allylamino-6-chloro-1,3,5-triazine and 14.74 g (0.08 mole) of 2-(2,2,6,6-tetramethylpiperid-4-yl)-ethylamine in 130 ml of xylene are heated at reflux temperature for 4 hours, while stirring. 3.5 g (0.088 mole) of finely powdered sodium hydroxides are then added to the reaction mixture in 4 portions over a period of 4 hours, and the mixture is kept at reflux temperature overnight. The reaction mixture is then freed from the precipitated sodium chloride by filtration while hot, the xylene is completely removed by vacuum distillation, and the residue is recrystallised from n-pentane. The 2,4-bis-allylamino-6-[2-(2,2,6,6-tetramethylpiperid-4-yl)-ethylamino]-1,3,5-triazine thus obtained has a melting point of 74°-75° (stabiliser No. 14).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04731393
Source datasetuspto-grants-1988_03
ORD IDord-803457f9cb924565ad9e82f8b0037346
Source noteuspto-grants-1988_03