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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569195Generated: November 3, 2026

Allylamine → HCID 20148735, compound

https://huagongshe.com/reaction/569195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylamineHCID 7853—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 21468019HCID 21468019—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 20148735HCID 20148735—

Reaction Steps

17.2 g (0.3 mole) of anhydrous allylamine are added dropwise, in the course of one hour, at 30°-40° and while stirring, to a solution of 103.6 g (0.15 mole) of N,N'-bis-(2,4-dichloro-1,3,5-triazin-6-yl)-N,N'-bis-(2,2,6,6-tetramethylpiperid-4-yl)-hexamethylenediamine in 500 ml of toluene. A solution of 12.0 g (0.3 mole) of sodium hydroxide in 100 ml of water is then added at approx. 30°, and stirring is continued for a further 19 hours at 50°. The mixture is worked up by separating off the aqueous phase in a separating funnel, washing the organic phase with three times 200 ml of water, drying it over sodium sulfate and removing the solvent by vacuum distillation. The solid residue is recrystallised from ethyl methyl ketone, which gives pure N,N'-bis-(2-chloro-4-allylamino-1,3,5-triazin-6-yl)-N,N'-bis-(2,2,6,6-tetramethylpiperid-4-yl)-hexamethylenediamine of melting point 210°-211°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04731393
Source datasetuspto-grants-1988_03
ORD IDord-46754e814ff042cca44c5ee8b035efcf
Source noteuspto-grants-1988_03