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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380394Generated: October 26, 2026

p-Toluidine → 1-(Methylamino)-4-((4-methylphenyl)amino)anthraquinone

https://huagongshe.com/reaction/2380394

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-ToluidineHCID 7813—
Reactant9,10-Anthracenedione, 1-bromo-4-(methylamino)-HCID 31418—
ReactantSodium AcetateHCID 517045—
CatalystCupric acetateHCID 8895—
SolventMethanolHCID 887—
Product1-(Methylamino)-4-((4-methylphenyl)amino)anthraquinoneHCID 6719582%

Reaction Steps

In a reactor were charged p-toluidine (80 parts) , 1-methylamino-4-bromoanthraquinone (15.8 parts), sodium acetate (7.5 parts) and copper acetate (0.5 part) and the mixture was kept at 115° to 120° C. for 6 hours under a nitrogen atmosphere. Thereafter, the reaction mixture was diluted with methanol (100 parts) and cooled. The precipitate produced was filtrated, washed with methanol (500 parts) and then water (200 parts), and dried at 80° to 90° C. to obtain 1-methylamino-4- (4 '-methylanilino) -anthraquinone (yield 82% ).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05367075
Source datasetuspto-grants-1994_11
ORD IDord-afd62127cb4647ccb6659aacef3f72ed
Source noteuspto-grants-1994_11