Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 5-Nitro-1,4,4a,9a-tetrahydroanthraquinone | HCID 10868940 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Aminoanthraquinone | HCID 6710 | — |
Reaction Steps
A mixture of 5.0 parts of 5-nitro-1,4,4a,9a-tetrahydroanthraquinone with 50 parts of pyridine was stirred at 90°C for 2 hours with introducing thereinto 0.8 parts/hour of gaseous hydrogen sulfide. The reaction mixture was then cooled to 25°C and added with 50 parts of water to precipitate crystals. The crystals were recovered by filtration, washed with water and dried under reduced pressure to obtain 3.9 parts of 1-aminoanthraquinone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03966775 |
|---|
| Source dataset | uspto-grants-1976_06 |
|---|
| ORD ID | ord-4446aae9b73848579356cfdb51b618b9 |
|---|
| Source note | uspto-grants-1976_06 |
|---|