HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-Nitroanthraquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Nitroanthraquinone | HCID 6704 | — |
| Reactant | 1-Aminoanthraquinone | HCID 6710 | — |
| Reactant | Potassium Sulfide | HCID 162263 | — |
| Product | 1-Nitroanthraquinone | HCID 6704 | — |
| Product | 1-Aminoanthraquinone | HCID 6710 | — |
| Product | HCID 15570414 | HCID 15570414 | — |
Reaction Steps
The manufacture of 1-aminoanthraquinones by the reduction of 1-nitroanthraquinone has already been described. Beisler, Jones, Am. Soc. 44, 2304, were able to reduce 1-nitroanthraquinone to 1-aminoanthraquinone by treatment with potassium sulphide in boiling water. On the other hand, 1-aminoanthraquinone and 1-hydroxy-aminoanthraquinone result side by side in the reduction of 1-nitroanthraquinone dissolved in benzene with NaHS in an aqueous calcium chloride solution (Haworth, Lapworth, Soc. 119, 774).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04021456 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-baf9f6bdfc7942029d1235f89efd9d45 |
| Source note | uspto-grants-1977_05 |