HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2256079Erstellt: 26. Oktober 2026
Ethanol → 6-Benzyl-5,7-dihydro-5,7-dioxopyrrolo[3,4-b]pyridine
https://huagongshe.com/reaction/2256079
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethanol | HCID 702 | — |
| Edukt | Benzylamine | HCID 7504 | — |
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Produkt | 6-Benzyl-5,7-dihydro-5,7-dioxopyrrolo[3,4-b]pyridine | HCID 289502 | — |
Reaktionsschritte
To 100 g of 2,3-pyridinedicarboxylic acid was added dropwise 170 ml of acetic anhydride at room temperature, and the mixture was heated up to 110° C., and stirred for 4 hours. After completion of the reaction, the solvent was removed under reduced pressure. To a residue was added 200 ml of diethyI ether, and a precipitated crystal was collected by filtration and washed with diethyl ether (100 ml×4) to yield 86 g of an acid anhydride compound. To the product was added dropwise 76 ml of benzylamine while cooling with ice, and the mixture was stirred at 180° C. for 30 minutes. To the reaction mixture was added dropwise 170 ml of acetic anhydride while cooling with ice, followed by stirring at 110° C. for 2 hours. After completion of the reaction, the reaction mixture was allowed to cool, and 500 ml of ethanol was added thereto. The thus formed crystal was collected by filtration and washed with ethanol (100 ml×3) to yield 89.4 g of the titled compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05654318 |
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| Quelldatensatz | uspto-grants-1997_08 |
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| ORD ID | ord-3de2991fa53d4da091552e36152d18d5 |
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| Quellennotiz | uspto-grants-1997_08 |
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