Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40424Generated: October 25, 2026

Cyanuric chloride → N,N',N''-trioctadecyl-1,3,5-triazine-2,4,6-triamine

https://huagongshe.com/reaction/40424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanuric chlorideHCID 7954—
ReactantOctadecylamineHCID 15793—
Reactant1-Methoxy-3-(3-methoxypropoxy)propaneHCID 86302—
ReactantSodium AcetateHCID 517045—
SolventAcetic AcidHCID 176—
SolventIsopropanolHCID 3776—
ProductN,N',N''-trioctadecyl-1,3,5-triazine-2,4,6-triamineHCID 21758268—

Reaction Conditions

Temperature85 °C

Reaction Steps

Under a nitrogen atmosphere, a mixture of octadecylamine (389 grams, 1.44 mol), di(propylene glycol) dimethyl ether (1.50 liters), sodium acetate (134 grams, 1.63 mol), and cyanuric chloride (88.4 grams, 0.479 mol) was stirred for thirty minutes and then heated to 85° C. for two hours. The reaction mixture was heated to 155° C. at which temperature acetic acid was allowed to reflux out of the reaction mixture. The reaction mixture was heated to 170° C. for sixteen hours. 2-Propanol (1.60 liters) was added to the reaction mixture when it had cooled to 80° C. The precipitate was filtered at room temperature and washed with excess 2-propanol. The solid was stirred in refluxing water (2.00 liters) for two hours, filtered, and washed with excess water. The solid was stirred in refluxing 2-propanol (2.00 liters), filtered, and washed with excess 2-propanol to yield 377 grams of N,N′,N″-trioctadecyl-1,3,5-triazine-2,4,6-triamine as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08529671B2
Source datasetuspto-grants-2013_09
ORD IDord-c1c824e4b36c4c7fa0cf2336fe534b7b
Source noteuspto-grants-2013_09