HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → 1-Phenoxyanthracene-9,10-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | 1-Amino-2-bromo-4-hydroxyanthraquinone | HCID 8320 | — |
| Reactant | Disperse Red 60 | HCID 28531 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 1-Phenoxyanthracene-9,10-dione | HCID 3550312 | — |
Reaction Steps
Ya. B. Shteinberg and S. S. Tkachenko, Zh. Prikl. Khim. 49 (1976) 4, 904-905, describe a process for the preparation of 1-amino-2-phenoxy-4-hydroxyanthraquinone in an aqueous medium. In this process, 1-amino-2-bromo-4-hydroxyanthraquinone is reacted with phenol in aqueous potassium hydroxide solution in the presence of dispersants at 150° C. The authors claim yields of 87-90%. On repeating this process with various dispersants, we were unable to obtain a phenoxyanthraquinone derivative which could be used as a dye. In every case, the content of 1-amino-2-phenoxy-4-hydroxyanthraquinone in the products was less than 80%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04278606 |
| Source dataset | uspto-grants-1981_07 |
| ORD ID | ord-b99688e19ca1420fb40923031c03e2da |
| Source note | uspto-grants-1981_07 |