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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 224516Erstellt: 24. Oktober 2026

1,5-Dichloroanthraquinone → 9,10-Anthracenedione, 1,5-bis(phenylthio)-

https://huagongshe.com/de/reaction/224516

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,5-DichloroanthraquinoneHCID 6711—
EduktThiophenolHCID 7969—
EduktPotassium CarbonateHCID 11430—
LösungsmittelMethanolHCID 887—
Produkt9,10-Anthracenedione, 1,5-bis(phenylthio)-HCID 91914—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

The yellow pleochroic 1,5-bis(phenylthio)anthraquinone was prepared as follows: Two equivalents (2.2 g) mercaptobenzene were added to 30 g NN'Dimethylformamide, 5 g potassium carbonate, one equivalent (2.7 g) 1,5-dichloroanthraquinone and heated to reflux for 4 hours, after which 100 ml methanol were added after cooling to 80° C. Upon collecting the crystalline product by filtration, chromatography on alumina using toluene-methanol, and drying, the bright yellow orange crystalline product was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04232949
Quelldatensatzuspto-grants-1980_11
ORD IDord-7b8ff800cdc545d8bbcbe9a696318655
Quellennotizuspto-grants-1980_11