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HRID 569194作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物N,N'-Diallyl-6-chloro-1,3,5-triazine-2,4-diamineHCID 27306—
反応物4-Piperidineethanamine, 2,2,6,6-tetramethyl-HCID 12567367—
溶媒O-XyleneHCID 7237—
生成物2,4-Bis-allylamino-6-[2-(2,2,6,6-tetramethylpiperid-4-yl)-ethylamino]-1,3,5-triazineHCID 70415291—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04731393
出典データセットuspto-grants-1988_03
ORD IDord-803457f9cb924565ad9e82f8b0037346
出典メモuspto-grants-1988_03