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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 258358Erstellt: 24. Oktober 2026

Cyanuric chloride → Anthraquinone

https://huagongshe.com/de/reaction/258358

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyanuric chlorideHCID 7954—
Edukt3-Aminobenzenesulfonic acidHCID 8474—
Edukt1-Amino-2-bromo-4-(3'-amino-4'-sulfophenylthio)anthraquinoneHCID 19737700—
ProduktAnthraquinoneHCID 6780—

Reaktionsschritte

1-Amino-2-bromo-4-(3'-amino-4'-sulfophenylthio)anthraquinone (10.1 parts), cyanuric chloride (3.7 parts) and 1-aminobenzene-4-β-sulfatoethylsulfone (5.6 parts) were subjected to condensation reactions one after another in an aqueous medium in a usual manner, followed by a condensation reaction with 3-aminobenzenesulfonic acid (3.5 parts) at 50° to 70° C. under a weak acid condition. Thereafter, salting out of the reaction mixture gave an anthraquinone compound of the following formula (free acid form). ##STR322##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05266696
Quelldatensatzuspto-grants-1993_11
ORD IDord-18d078d7c7ec46f5876ce6d7f1333931
Quellennotizuspto-grants-1993_11