Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Dipotassium Oxalate | HCID 11413 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 5-Nitro-1,10-phenanthroline | HCID 72790 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 4,5-Diazafluoren-9-one | HCID 342157 | 54% |
Reaktionsschritte
To a 1 L one-necked flask was added a mixture of 30 g (0.13 mol, 68%) 5-nitro-1,10-phenanthroline, 51 g (0.61 mol) potassium oxalate, 12.5% NaOH(aq) 150 ml and 450 ml water. The mixture was then heated to reflux (100° C.) and stirred for 2 hours. After completion of the reaction, the reaction mixture was cooled to room temperature. The reaction mixture was added with 1 L ethyl acetate, stirred for 30 minutes, and filtered to collect the filtrate. The residual solids were added into 300 ml ethyl acetate, stirred for 30 minutes and filtered to collect the filtrate. The combined filtrates were extracted to separate the organic layer, dehydrated by MgSO4, concentrated, and recrystallized from 200 ml methanol, so as to obtain light yellow solids cyclopenta[2,1-b;3,4-b′]dipyridin-5-one 13.3 g (0.07 mol, yield 54%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07282586B1 |
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| Quelldatensatz | uspto-grants-2007_10 |
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| ORD ID | ord-67cec32dc96f459abfdccf7df882b11c |
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| Quellennotiz | uspto-grants-2007_10 |
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