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HRID 1292552Erstellt: 25. Oktober 2026
(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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | (1S,2S)-1,2-diphenylethane-1,2-diamine | HCID 6931238 | — |
| Edukt | 2-Formyl-(2,4,6-trimethylphenyl)-1,3-dioxobutane | HCID 18915756 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Dichloromethane ether hexane | HCID 21850893 | — |
| Produkt | N,N'-bis[3-oxo-2-(2,4,6-trimethylbenzoyl)butylidene]-(1S,2S)-1,2-diphenylethylenediamine | HCID 86752666 | 71% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05756790 |
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| Quelldatensatz | uspto-grants-1998_05 |
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| ORD ID | ord-343eb5588b0d472983981067a741ecde |
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| Quellennotiz | uspto-grants-1998_05 |
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