HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanuric chloride → Anthraquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | 3-Aminobenzenesulfonic acid | HCID 8474 | — |
| Reactant | 1-Amino-2-(3'-amino-4'-sulfophenoxy)-4-(4-sulfophenylthio)anthraquinone | HCID 14717378 | — |
| Product | Anthraquinone | HCID 6780 | — |
Reaction Steps
1-Amino-2-(3'-amino-4'-sulfophenoxy)-4-(4'-sulfophenylthio)anthraquinone (6 parts), cyanuric chloride (1.8 parts) and 1-aminobenzene-4-β-sulfatoethylsulfone (2.8 parts) were subjected to condensation reactions one after another in an aqueous medium in a conventional manner, followed by a successive condensation reaction with 3-aminobenzenesulfonic acid (1.7 parts) at 50° to 70° C. under a weak acid condition. Thereafter, salting out of the reaction mixture gave an anthraquinone compound of following formula (free acid form). ##STR117##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05266696 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-ec448160f7474ac0a180e86215289add |
| Source note | uspto-grants-1993_11 |