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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196093Generated: November 1, 2026

Cyanuric chloride → Anthraquinone

https://huagongshe.com/reaction/1196093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanuric chlorideHCID 7954—
Reactant3-Aminobenzenesulfonic acidHCID 8474—
Reactant1-Amino-2-(3'-amino-4'-sulfophenoxy)-4-(4-sulfophenylthio)anthraquinoneHCID 14717378—
ProductAnthraquinoneHCID 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 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112971
Source datasetuspto-grants-1992_05
ORD IDord-4950e5d17f01474aac436f3ee4463bec
Source noteuspto-grants-1992_05