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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973001Generated: October 26, 2026

1-Nitroanthraquinone → 1-Aminoanthraquinone

https://huagongshe.com/reaction/973001

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NitroanthraquinoneHCID 6704—
Reactant9,10-Anthracenedione, 1,5-dinitro-HCID 6705—
ReactantAnthraquinoneHCID 6780—
ReactantSodium HydroxideHCID 14798—
Reactant1,8-Dinitro-9,10-anthraquinoneHCID 67210—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
Product1-AminoanthraquinoneHCID 671093%

Reaction Steps

A 500 ml. electromagnetically stirred autoclave was charged with 10 g of 1-nitroanthraquinone having a purity of 91.5% and containing 7.0% of 1,5-dinitroanthraquinone, 0.5% of 1,8-dinitroanthroquinone and 1.0% of anthraquinone as impurities, 120 g of a 3% aqueous solution of sodium hydroxide (0.01 mole as sodium hydroxide), 80 g of methanol, and 200 mg of 5% palladium-carbon (2% based on the 1-nitroanthraquinone). The 1-nitroanthraquinone was hydrogenated at a temperature of 50° C. and a pressure of 40 to 30 Kg/cm2.G. In 60 minutes, 0.16 mole of hydrogen was absorbed, whereupon the reaction was stopped. The inside of the autoclave was purged with nitrogen, and 80 g of a 3% aqueous solution of sodium hydroxide was added. Methanol was distilled off at reduced pressure (60 to 70 mmHg abs.) and 40 to 50° C. Then, the reaction mixture was suction-filtered in a stream of nitrogen to remove the catalyst and the diaminoanthraquinones. The filtrate was oxidized with air at 20 to 30° C. for 2 hours with stirring to afford 7.65 g of 1-aminoanthraquinone having a purity of 98% in a yield of 93% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04054586
Source datasetuspto-grants-1977_10
ORD IDord-4af893a741ef4904995f0a023caf9232
Source noteuspto-grants-1977_10