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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983657Generated: October 30, 2026

Hydrogen Peroxide → Quinacridone

https://huagongshe.com/reaction/983657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantAnthraquinoneHCID 6780—
ReactantSodium HydroxideHCID 14798—
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 (Luviskole 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. 50 g 50% aqueous sodium hydroxide are added. The mixture is stirred under a slow flow of nitrogen at 50-53° C. for one hour. 0.8 g anthraquinone mono sulfonic acid sodium salt is added as catalyst and the reaction mixture is heated to reflux for 10 minutes. 76 g of an aqueous 18.9% hydrogen peroxide solution are added into the reaction mixture with a peristaltic pump at a pumping rate of 0.4 ml/minute. Then after 25 minutes addition time 1.6 g phthalimidomethyl-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 small particle size violet beta quinacridone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864371B2
Source datasetuspto-grants-2005_03
ORD IDord-f653d5e768154dee9be98336386e70a4
Source noteuspto-grants-2005_03