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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976122Generated: October 30, 2026

Sodium Hydroxide → Quinacridone

https://huagongshe.com/reaction/976122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium 3-nitrobenzenesulfonateHCID 31389—
ReactantQuino(2,3-b)acridine-7,14-dione, 5,6,12,13-tetrahydro-HCID 79973—
SolventMethanolHCID 887—
ProductQuinacridoneHCID 13976—

Reaction Conditions

Temperature40 °C

Reaction Steps

79 Parts of methanol and 12 parts of a 50% NaOH aqueous solution were fully stirred in a stainless steel flask having a refluxing device. 10 Parts of the 6,13-dihydroquinacridone obtained in Example 1 and 10 parts of sodium m-nitrobenzenesulfonate were gradually mixed with the above-prepared solution, and the mixture was refluxed at 70° to 75° C. for 3 to 5 hours. The reaction mixture was cooled to 40° C. and filtered, and the resultant cake was cleaned with hot water until a wash liquid became colorless and transparent, to give 9.77 parts (98.3% of a theoretical value) of a nonsubstituted quinacridone. The so-obtained quinacridone was measured by IR and absorbance to show 99.2% of quinacridone and 0.8% of 6,13-dihydroquinacridone. The quinacridone had a specific surface area of 22.1 m2 /g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05610306
Source datasetuspto-grants-1997_03
ORD IDord-7a6cb096bbc042858e95bb8fa78f4e12
Source noteuspto-grants-1997_03