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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983658Generated: November 2, 2026

Hydrogen Peroxide → Quinacridone

https://huagongshe.com/reaction/983658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantDisodium anthraquinone-2,7-disulfonateHCID 70069—
ReactantQuino(2,3-b)acridine-7,14-dione, 5,6,12,13-tetrahydro-HCID 79973—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductQuinacridoneHCID 13976—

Reaction Conditions

Temperature23.5 °C

Reaction Steps

A one liter flask equipped with a thermometer, stirrer and condenser is charged with 50 G 6,13-dihydroquinacridone, 200 ml methanol, 1 g polyvinyl pyrrolidone powder (Luviskol® K-30, BASF) and 7 g of the aqueous presscake of the nanosize quinacridone naphthalene sulfonic acid formaldehyde polymer mixture according to Example 2, are stirred at 20-27° C. for 10 minutes. 73 g 50% aqueous sodium hydroxide are added. The mixture is stirred under a slow flow of nitrogen at 50-53° C. for 30 minutes. 4.6 g of a 37% aqueous solution of anthraquinone-2,7-disulfonic acid disodium salt is added as catalyst followed by 10 ml water and the reaction mixture is heated to reflux for 40 minutes. 79 g of an aqueous 18.2% hydrogen peroxide solution are added into the reaction mixture with a peristaltic pump at a pumping rate of 0.4 ml/minute. Then after 20 minutes addition time 2.3 g phthalimido methyl-quinacridone and after another 70 minutes 0.3 g phthalimido methyl-quinacridone are introduced into the reaction mixture followed by continuing the hydrogen peroxide addition while maintaining reflux and a slow nitrogen flow. The resulting violet suspension is further stirred for 10 minutes at reflux then diluted with 100 ml cold water and filtered. The presscake is washed with hot water then dried, yielding a violet quinacridone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864371B2
Source datasetuspto-grants-2005_03
ORD IDord-d32dacfec31c4fab9a857b88758d4a0d
Source noteuspto-grants-2005_03