Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | N-Anthraquinon-1-ylacetamide | HCID 76760 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 1-Aminoanthraquinone | HCID 6710 | 95,2% |
Reaktionsschritte
363 g (1.37 moles) of 1-acetamino-anthraquinone are stirred into 3.5 kg of ethanol, 150 ml of concentrated sodium hydroxide solution (d = 1.48) are added and the mixture is then heated to the reflux temperature (80° C) for three hours. After cooling to 15° C, the red suspension is suction filtered. The residue is washed on the suction filter with hot water until the filtrate has a neutral reaction. After drying, 291 g of 1-amino-anthraquinone are obtained (yield: 95.2%). Degree of purity: 98 to 99%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US03997573 |
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| Quelldatensatz | uspto-grants-1976_12 |
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| ORD ID | ord-8e533b09755141eeb8097976c434c77c |
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| Quellennotiz | uspto-grants-1976_12 |
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