HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 1-Aminoanthraquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 2-Anthracenecarboxylic acid, 1-amino-9,10-dihydro-9,10-dioxo- | HCID 6701 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Aminoanthraquinone | HCID 6710 | 83.3% |
Reaction Steps
To a three-necked round-bottomed flask equipped with stirrer and reflux condenser was added 2 g (0.007 mole) 1-aminoanthraquinone-2-carboxylic acid, 0.5 g (0.0018) zinc dust, 5 ml of 30% ammonium hydroxide solution and 30 ml of water. The resulting mixture was refluxed gently until evolution of carbon dioxide ceased, ca. 30 minutes. The mixture was then filtered while hot, and the filter cake was washed with water. The wet cake containing the zinc catalyst was heated over a steam bath with 50% sulfuric acid for one hour. Water was added and the solid product was collected by filtration and washed with water until acid-free. The product was dried to give 1.3 g (83.3% yield) of more than 90% pure 1-aminoanthraquinone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04328160 |
| Source dataset | uspto-grants-1982_05 |
| ORD ID | ord-679e3688a90d4ce6925eb4f37512933f |
| Source note | uspto-grants-1982_05 |