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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110947Generated: November 2, 2026

Cyanuric chloride → Anthraquinone

https://huagongshe.com/reaction/1110947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanuric chlorideHCID 7954—
Reactant1-Amino-4-(3-amino-2,4,6-trimethyl-5-sulphoanilino)-9,10-dihydro-9,10-dioxoanthracene-2-sulphonic acidHCID 90368—
ProductAnthraquinoneHCID 6780—

Reaction Steps

1-Amino-4-(3'-amino-2',4',6'-trimethyl-5'-sulfoanilino)anthraquinone-2-sulfonic acid (23.7 parts), cyanuric chloride (9.3 parts) and 1-aminobenzene-4-β-sulfatoethylsulfone (14.1 parts) were subjected to condensation in an aqueous medium one after another in a usual manner. Successively, the condensate was allowed to react with 1-aminobenzene-3-β-sulfatoethylsulfone (14.1 parts) at 60° to 70° C. under a weak acid condition. Thereafter, the reaction mixture was salted-out to separate crystals, thereby obtaining an anthraquinone compound of the following formula in the free acid form. ##STR24##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977261
Source datasetuspto-grants-1990_12
ORD IDord-3d44f83f313e4ca3a5d48d1d54ff4c6c
Source noteuspto-grants-1990_12