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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070356Generated: October 31, 2026

Hydrogen Peroxide → Quinacridone

https://huagongshe.com/reaction/1070356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantQuino(2,3-b)acridine-7,14-dione, 5,6,12,13-tetrahydro-HCID 79973—
ReactantHCID 131724965HCID 131724965—
CatalystAnthraquinoneHCID 6780—
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 polyvinylpyrrolidone 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 1 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 as catalyst is added and the reaction mixture is heated to reflux for 10 minutes. 76 g of an aqueous 18.9% by weight hydrogen peroxide solution are added into the reaction mixture with a peristaltic pump at a pumping rate of 0.4 ml/minute, whereby 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 violet quinacridone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06902613B2
Source datasetuspto-grants-2005_06
ORD IDord-a250d0997c924a3f9d1e40cc1631d062
Source noteuspto-grants-2005_06