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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258366Generated: October 28, 2026

Cyanuric chloride → Anthraquinone

https://huagongshe.com/reaction/258366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanuric chlorideHCID 7954—
Reactant3-Aminobenzenesulfonic acidHCID 8474—
ReactantHCID 15076661HCID 15076661—
ProductAnthraquinoneHCID 6780—

Reaction Steps

1-Amino-4-(3'-amino-2',4',6'-trimethyl-5'-sulfophenylthio)anthraquinone-2-sulfonic acid (23.7 parts), cyanuric chloride (9.3 parts) and 1-aminobenzene-3-β-sulfatoethylsulfone (14.1 parts) were subjected to condensation reactions one after another in an aqueous medium in a usual manner, followed by a further condensation reaction with 3-aminobenzenesulfonic acid (8.7 parts) at 50° to 60° C. under a weak acid condition. Thereafter, salting out of the reaction mixture gave an anthraquinone compound of the following formula (free acid form). ##STR519##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05266696
Source datasetuspto-grants-1993_11
ORD IDord-049af25bca7249b7885a6dd2aa074493
Source noteuspto-grants-1993_11