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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1196103Erstellt: 25. Oktober 2026

Methanol → Anthraquinone

https://huagongshe.com/reaction/1196103

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktPotassium CarbonateHCID 11430—
Edukt1-Amino-4-bromo-9,10-dioxo-9,10-dihydroanthracene-2-carboxylic acidHCID 271593—
Edukt4-(4'-beta-Hydroxyethylsulfonylphenoxy)thiophenolHCID 19737697—
Lösungsmittel1,2-DichlorobenzeneHCID 7239—
ProduktAnthraquinoneHCID 6780—

Reaktionsschritte

1-Amino-2-carboxy-4-bromoanthraquinone (6.9 parts) and 4-(4'-β-hydroxyethylsulfonylphenoxy)thiophenol (6.5 parts) were allowed to react with each other at 100° to 120° C. in 0-dichlorobenzene in the presence of cuprous chloride and potassium carbonate. Thereafter, methanol was added to the reaction mixture to deposit solids, which were collected on a filter, washed throughly with methanol and water and then dried at 80° C. The resulting product was subjected to sulfonation and esterification simultaneously at 20° to 40° C. in 14% oleum. Thereafter, ice was added thereto, the solids deposited were collected on a filter, thereby obtaining an anthraquinone compound of the following formula (free acid form). ##STR383##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05112971
Quelldatensatzuspto-grants-1992_05
ORD IDord-2355d823ccc34be098d97875345f48ed
Quellennotizuspto-grants-1992_05