Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 21292556 | HCID 21292556 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178514954 | HCID 178514954 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | 1-Aminoanthraquinone | HCID 6710 | 97.5% |
Reaction Steps
To a mixture of 260 grams of 5-nitrotetrahydroanthraquinone and 10,100 grams of methyl cellosolve were added 2.6 grams of a 5% palladium on carbon catalyst and 300 grams of a 20% aqueous sodium hydroxide solution, followed by agitating at room temperature for 1 hour. The color of the solution was green inherent to 1-hydroxylaminoanthraquinone. Part of the reaction solution was sampled and subjected to a thin layer chromatography, by which it was recognized that almost all of the starting 5-nitro compound was converted to 1-hydroxylaminoanthraquinone. Thereafter, hydrogen was fed into the reaction solution for hydrogenation and 2 mols of hydrogen was absorbed in each 1 mol of the 5-nitro compound. The hydrogen in the reactor was replaced by nitrogen, followed by introduction of air into the reaction solution for oxidation. Upon determination, it was found that oxygen was absorbed in an amount of 0.5 mol per mol of the 5-nitro compound. The reaction solution turned reddish orange with a reddish orange precipitate. The precipitate was separated by filtration, washed with water and dried to obtain 220 grams of 1-aminoanthraquinone having a purity of 98%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03994932 |
|---|
| Source dataset | uspto-grants-1976_11 |
|---|
| ORD ID | ord-5594a208acbe4480a9a3a50a31d7a68f |
|---|
| Source note | uspto-grants-1976_11 |
|---|