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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731008Generated: October 31, 2026

Cyclohexanol → 1-Aminoanthraquinone

https://huagongshe.com/reaction/1731008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanolHCID 7966—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 21292556HCID 21292556—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
Product1-AminoanthraquinoneHCID 671082.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

3 Grams of a Raney nickel catalyst and 100 grams of a 20% aqueous sodium hydroxide solution were added to a mixture of 128 grams of 5-nitrotetrahydroanthraquinone and 1,700 grams of cyclohexanol, into which was fed hydrogen while agitating at 100° C. for having hydrogen absorbed in the starting 5-nitro compound in an amount of 2 mols per mol of the 5-nitro compound. After completion of hydrogenation, the catalyst was separated by filtration and air was passed into the resultant filtrate at 30° C. for 1 hour. The resultant solution was cooled to 10° C. to precipitate crystals, which were then separated by filtration, washed with water and dried to obtain 92 grams of 1-aminoanthraquinone having a purity of 98.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03994932
Source datasetuspto-grants-1976_11
ORD IDord-72e00d43b01645bdb8b0c3e08c2b688d
Source noteuspto-grants-1976_11