戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1292552作成日:2026年10月26日

(1S,2S)-1,2-diphenylethane-1,2-diamine → N,N'-bis[3-oxo-2-(2,4,6-trimethylbenzoyl)butylidene]-(1S,2S)-1,2-diphenylethylenediamine

https://huagongshe.com/reaction/1292552

反応式

関与物質

役割名称HCID仕込み量
反応物(1S,2S)-1,2-diphenylethane-1,2-diamineHCID 6931238—
反応物2-Formyl-(2,4,6-trimethylphenyl)-1,3-dioxobutaneHCID 18915756—
溶媒EthanolHCID 702—
溶媒Dichloromethane ether hexaneHCID 21850893—
生成物N,N'-bis[3-oxo-2-(2,4,6-trimethylbenzoyl)butylidene]-(1S,2S)-1,2-diphenylethylenediamineHCID 8675266671%

反応手順

In 70 ml of ethanol was dissolved 1.06 g (5 mmol) of (S,S)-1,2-diphenylethylenediamine. In a nitrogen atmosphere and at room temperature, 30 ml of an ethanol solution containing 2.32 g (10.5 mmol) of 2-formyl-(2,4,6-trimethylphenyl)-1,3-dioxobutane was added to the solution, which was stirred for 2 hours at room temperature. The reaction mixture was then heated to 50° C. and reaction took place in 2 hours. After the completion of reaction, the solvent was distilled off in vacuum, obtaining a crude product. The crude product was dissolved in dichloromethane/ether/hexane for recrystallization, obtaining 2.28 g (isolation yield 71%) of an optically active ligand (N,N'-bis[3-oxo-2-(2,4,6-trimethylbenzoyl)butylidene]-(1S,2S)-1,2-diphenylethylenediamine) as white crystals. The thus obtained optically active ligand was analyzed by 1H-NMR, IR, and elemental analysis and measured for melting point and specific rotatory power. The results are shown below.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05756790
出典データセットuspto-grants-1998_05
ORD IDord-343eb5588b0d472983981067a741ecde
出典メモuspto-grants-1998_05