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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 569192생성일: 2026년 10월 25일

Allylamine → N,N'-Diallyl-6-chloro-1,3,5-triazine-2,4-diamine

https://huagongshe.com/reaction/569192

반응식

참여 물질

역할이름HCID투입량
반응물AllylamineHCID 7853—
반응물Cyanuric chlorideHCID 7954—
반응물Sodium HydroxideHCID 14798—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물N,N'-Diallyl-6-chloro-1,3,5-triazine-2,4-diamineHCID 27306—

반응 단계

54.9 g (0.96 mole) of allylamine are added dropwise, in the course of 1.5 hours and while stirring, to a clear solution of 73.8 g (0.4 mole) of cyanuric chloride in 500 ml of toluene, the temperature being kept between 20° and 30° by applying gentle external cooling to the reaction vessel. After stirring for a further two hours at room temperature and for one hour at 50°, the mixture is cooled to 20°, and a solution of 16 g (0.4 mole) of sodium hydroxide in 70 ml of water is added dropwise at 20° in the course of 2 hours. After stirring for a further 2 hours at room temperature and for 6 hours at 60°, a further 16 g (0.4 mole) of sodium hydroxide in 70 ml of water are added dropwise in the course of 2 hours and stirring is continued for a further 5 hours at 60°. After the mixture has cooled to room temperature, 200 ml of water are added, and the precipitate is filtered off after stirring for approx. 30 minutes. The precipitate is thoroughly washed with water, thoroughly suction-drained and dried in vacuo at approx. 95°. The colourless 2,4-bis-allylamino-6-chloro-1,3,5-triazine thus obtained is analytically pure and has a melting point of 205°-206°; its water content is <0.3%. Yield 88.2 g (97.7% of theory).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04731393
출처 데이터셋uspto-grants-1988_03
ORD IDord-e1b08bff97b54b80b36fe02999720db6
출처 메모uspto-grants-1988_03