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HRID 255846Erstellt: 25. Oktober 2026

Pyridine → 1,4-Diamino-9,10-dihydro-9,10-dioxoanthracene-2-sulphonic acid

https://huagongshe.com/reaction/255846

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktFuming sulfuric acidHCID 24681—
EduktDisperse Violet 1HCID 31420—
LösungsmittelWaterHCID 962—
Produkt1,4-Diamino-9,10-dihydro-9,10-dioxoanthracene-2-sulphonic acidHCID 7772585%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

60 parts of 1,4-diaminoanthraquinone are added to 228 parts of 25% oleum over one hour and then 20 parts of pyridine are added. The temperature of the reaction mixture is 70°-80° C. and is further raised to 120° C. The reaction mixture is stirred at this temperature for 3 hours, then cooled to 70°-80° C., and 220 parts of water are slowly added dropwise. The resultant thick suspension is filtered at room temperature and the filter cake is washed with 100 parts of 50% sulfuric acid and subsequently dispersed in water. The pH of the aqueous suspension is then adjusted to 7.5 with 35% sodium hydroxide solution, whereupon the 1,4-diaminoanthraquinone-2sulfonic acid goes into solution. The solution is then heated to 85°-90° C. and 40 parts of magnesium sulfate are added. Upon cooling the reaction solution, the 1,4-diaminoanthraquinone-2-sulfonic acid crystallises in the form of the magnesium salt, which is isolated by filtration, washed with a 5% solution of magnesium sulfate and dried, affording 72.4 parts of the magnesium salt of 1,4-diaminoanthraquinone-2-sulfonic acid, corresponding to a yield of 85%. According to chromatographic analysis, the product is homogeneous with a trace of starting material. The Rf value is 0.57, which confirms that this product is identical with that obtained in Example 1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04699735
Quelldatensatzuspto-grants-1987_10
ORD IDord-1d98f2ab2e504a8d9ae12b84ca777f41
Quellennotizuspto-grants-1987_10