Water → 2,4,6-Trimethylmelamine
反応式
[N:1]1C(Cl)=NC(Cl)=N[C:2]=1Cl.CN.O.C(=O)([O-])O.[K+].[CH3:18][NH:19][C:20]1[N:25]=[C:24]([NH:26][CH3:27])[N:23]=[C:22](Cl)[N:21]=1>C(#N)C>[CH3:18][NH:19][C:20]1[N:25]=[C:24]([NH:26][CH3:27])[N:23]=[C:22]([NH:1][CH3:2])[N:21]=1参加物
反応条件
- 温度
- 0 °C
実験手順
After 18.5 g (0.1 mol) of cyanuric chloride was dissolved into 150 ml of acetonitrile, the resulting mixture was cooled to 0° C. and 15.5 g (0.2 mol) of 40% aqueous solution of methylamine was added dropwise in 1 hour thereto under stirring in such a manner that the reaction temperature did not exceed 5° C. While further stirring, 100 ml of water including 20.0 g (0.2 mol) of potassium hydrogencarbonate was added dropwise at the same temperature. Thereafter, the reaction temperature was gradually raised, and stirred at 45° C. for 8 hours. After confirming that an inversion to 2.4-bis(methylamino)-6-chloro-1,3,5-triazine was completed, the reaction solution was cooled and products were filtered off. The filter cake was fully washed with water, and then the resulting 2,4-bis(methylamino)-6-chloro-1,3,5-triazine was suspended into 100 ml of water, and 31.1 g (0.4 mol) of 40% aqueous solution of methylamine was added, and further heated under reflux for 6 hours. After cooling, the deposited crystal was filtered, washed fully with water and dried to give 13.1 g (yield: 78%) of the titled compound. Melting point 133° C.
後処理
- customdid not exceed 5° C
- temperatureThereafter, the reaction temperature was gradually raised
- stirringstirred at 45° C. for 8 hours
- temperaturethe reaction solution was cooled
- filtrationproducts were filtered off
- washThe filter cake was fully washed with water
- additionwas added
- temperaturefurther heated
- temperatureunder reflux for 6 hours
- temperatureAfter cooling
- filtrationthe deposited crystal was filtered
- washwashed fully with water
- customdried
出典と根拠
- ORDレコード
- ord-b3c50debf34447fbbf8f0bcf658de754
- 出典データセット
- uspto-grants-2005_04
- 特許番号
- US06878824B2
反応ノート
読み込み中…