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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071312Generated: November 2, 2026

Sodium Hydroxide → 1,2-Diaminoanthraquinone

https://huagongshe.com/reaction/2071312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant9,10-Anthracenedione, 1,2-dinitro-HCID 42596—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
Product1,2-DiaminoanthraquinoneHCID 1565298%

Reaction Steps

A 500 ml. electromagnetically stirred glass reactor was charged with 5.0 g (0.0167 mole) of dinitroanthraquinone (a mixture of 1,5-isomer and 1,8-isomer), 100 g (0.1 mole) of a 4% aqueous solution of sodium hydroxide and 0.25 g of 5% palladium-carbon. The inside of the reactor was purged with hydrogen, and the dinitroanthraquinone was hydrogenated at 30° C. with stirring. In 5 hours, 0.1169 mole of hydrogen was absorbed, the reaction was stopped. The reaction mixture was filtered in an atmosphere of nitrogen to separate the catalyst. Then, the filtrate was oxidized with air with stirring at 20° to 30° C. for 2 hours. The resulting crystals were filtered and dried to afford 3.9 g of diaminoanthraquinone (a mixture of 1,5-isomer and 1,8-isomer) in a yield of 97.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04046785
Source datasetuspto-grants-1977_09
ORD IDord-66190b0bac3540ceb1333c108bd123d4
Source noteuspto-grants-1977_09