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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163617Generated: November 1, 2026

Hexylamine → N~2~-Hexyl-1,3,5-triazine-2,4,6-triamine

https://huagongshe.com/reaction/2163617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexylamineHCID 8102—
ReactantSodium CarbonateHCID 10340—
Reactant1,3,5-Triazine-2,4-diamine, 6-chloro-HCID 18831—
SolventDimethylformamideHCID 6228—
ProductN~2~-Hexyl-1,3,5-triazine-2,4,6-triamineHCID 19734692—

Reaction Steps

A mixture of 72.8 g. (0.500 mole) of 2,4-diamino-6-chloro-s-triazine, 63.6 g. (0.600 mole) of anhydrous sodium carbonate, and 200 ml. of N,N-dimethylformamide (DMF) was heated over 43 minutes of 124° C. To this was added, over a period of 2.35 hours, a solution of 60.7 g. (0.600 mole) of n-hexylamine in 100 ml. of DMF; temperature was controlled at 122°-127° C. during the addition. The reaction mixture was heated for an additional 19 hours at 124°-125° C., then was filtered hot. The filter cake was washed with 100 ml of hot DMF, and the combined filtrate was cooled and added with stirring to about 5 liters of ice-water. The precipitate was recovered by filtration, reslurried with 3 liters of water, filtered again, washed thoroughly with deionized water, and dried to constant weight in a vacuum oven at 60° C. The yield of n-hexylmelamine, m.p. 115°-117.5° C., was 91.4 g. (87.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04136092
Source datasetuspto-grants-1979_01
ORD IDord-6907d8de27b74d2596a39b1ffe679d7e
Source noteuspto-grants-1979_01