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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731001Generated: November 1, 2026

Oxygen → 1-Aminoanthraquinone

https://huagongshe.com/reaction/1731001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 21292556HCID 21292556—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178514954HCID 178514954—
CatalystPalladiumHCID 23938—
Solvent2-MethoxyethanolHCID 8019—
Product1-AminoanthraquinoneHCID 671097.5%

Reaction Steps

To a mixture of 260 grams of 5-nitrotetrahydroanthraquinone and 10,100 grams of methyl cellosolve were added 2.6 grams of a 5% palladium on carbon catalyst and 300 grams of a 20% aqueous sodium hydroxide solution, followed by agitating at room temperature for 1 hour. The color of the solution was green inherent to 1-hydroxylaminoanthraquinone. Part of the reaction solution was sampled and subjected to a thin layer chromatography, by which it was recognized that almost all of the starting 5-nitro compound was converted to 1-hydroxylaminoanthraquinone. Thereafter, hydrogen was fed into the reaction solution for hydrogenation and 2 mols of hydrogen was absorbed in each 1 mol of the 5-nitro compound. The hydrogen in the reactor was replaced by nitrogen, followed by introduction of air into the reaction solution for oxidation. Upon determination, it was found that oxygen was absorbed in an amount of 0.5 mol per mol of the 5-nitro compound. The reaction solution turned reddish orange with a reddish orange precipitate. The precipitate was separated by filtration, washed with water and dried to obtain 220 grams of 1-aminoanthraquinone having a purity of 98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03994932
Source datasetuspto-grants-1976_11
ORD IDord-5594a208acbe4480a9a3a50a31d7a68f
Source noteuspto-grants-1976_11