HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2071313Erstellt: 24. Oktober 2026
Sodium Hydroxide → 2-Anthracenecarboxylic acid, 1-amino-9,10-dihydro-9,10-dioxo-
https://huagongshe.com/de/reaction/2071313
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 1-Nitroanthraquinone-2-carboxylic acid | HCID 31413 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Katalysator | HCID 178418390 | HCID 178418390 | — |
| Produkt | 2-Anthracenecarboxylic acid, 1-amino-9,10-dihydro-9,10-dioxo- | HCID 6701 | 91,3% |
Reaktionsschritte
A 500 ml. electromagnetically stirred glass reactor was charged with 5.0 g (0.0168 mole) of 1-nitro-2-carboxyanthraquinone, 100 g of a 4% aqueous solution of sodium hydroxide and 0.25 g of 5% palladium-carbon. The inside of the reactor was purged with hydrogen, and the 1-nitro-2-carboxyanthraquinone was hydrogenated at 50° C. with stirring. In 5 hours, 0.0504 mole of hydrogen was absorbed, whereupon the reaction was stopped. The reaction mixture was filtered to separate the catalyst. The filtrate was oxidized with air with stirring at 20° to 30° C. for 2 hours, and then neutralized with 20% sulfuric acid to a pH of 2 to 3. The crystals precipitated were filtered, washed with water, and dried to afford 4.1 g of 1-amino-2-carboxyanthraquinone in a yield of 91.3%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04046785 |
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| Quelldatensatz | uspto-grants-1977_09 |
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| ORD ID | ord-b7b4ae0a3b184a14b2178241f2244a20 |
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| Quellennotiz | uspto-grants-1977_09 |
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