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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731000Generated: November 3, 2026

Cyclohexanol → 1-Aminoanthraquinone

https://huagongshe.com/reaction/1731000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanolHCID 7966—
ReactantHCID 21292556HCID 21292556—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
Product1-AminoanthraquinoneHCID 671082.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 12.8 grams of 5-nitrotetrahydroanthraquinone and 170 grams of cyclohexanol was added 0.3 gram of a Raney-nickel catalyst. Then, hydrogen was fed into the mixture while agitating at 100° C. for hydrogenation. After hydrogen was absorbed in an amount of 2 mols per mol of the nitro compound, the catalyst was separated by filtration. To the resultant filtrate was added 10 grams of a 20% aqueous sodium hydroxide solution, followed by agitating at 100° C. for 1 hour. Then, the reaction solution was cooled to 10° C. to precipitate crystals which were separated by filtration, washed with water and dried to obtain 9.2 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-eb559aae455e48709e61281e63992933
Source noteuspto-grants-1976_11