化工社化工社 化学情報印刷レポート · 研究参考用
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
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-diamine | HCID 27306 | — |
| 反応物 | 4-Piperidineethanamine, 2,2,6,6-tetramethyl- | HCID 12567367 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | 2,4-Bis-allylamino-6-[2-(2,2,6,6-tetramethylpiperid-4-yl)-ethylamino]-1,3,5-triazine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04731393 |
|---|
| 出典データセット | uspto-grants-1988_03 |
|---|
| ORD ID | ord-803457f9cb924565ad9e82f8b0037346 |
|---|
| 出典メモ | uspto-grants-1988_03 |
|---|