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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 569194생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물N,N'-Diallyl-6-chloro-1,3,5-triazine-2,4-diamineHCID 27306—
반응물4-Piperidineethanamine, 2,2,6,6-tetramethyl-HCID 12567367—
용매O-XyleneHCID 7237—
생성물2,4-Bis-allylamino-6-[2-(2,2,6,6-tetramethylpiperid-4-yl)-ethylamino]-1,3,5-triazineHCID 70415291—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04731393
출처 데이터셋uspto-grants-1988_03
ORD IDord-803457f9cb924565ad9e82f8b0037346
출처 메모uspto-grants-1988_03