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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579667Generated: November 3, 2026

Methane → 1-Aminoanthraquinone

https://huagongshe.com/reaction/1579667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
Reactant1-NitroanthraquinoneHCID 6704—
ReactantAnisoleHCID 7519—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Product1-AminoanthraquinoneHCID 671095.1%

Reaction Steps

1 Part of nitroanthraquinone with a content of 97.0 percent of 1-nitroanthraquinone, 9 parts of anisole and 0.005 parts of catalyst (10 percent Pd on active charcoal) are heated to 130° in an autoclave with a capacity of 20 parts by volume and equipped with a rotary agitator. While heating, rinsing with nitrogen is effected and, on reaching the reaction temperature, hydrogen is passed through to provide a total pressure of 6.0 kp per cm2, at which the agitator is activated and hydrogenation effected until an amount of hydrogen corresponding to 264 parts by volume is taken up. The hydrogen is now followed by nitrogen and the catalyst separated, the filtrate cooled down to room temperature, when 1-aminoanthraquinone is formed in easily filtrable crystals. The crystallization product is separated, washed with a small quantity of cold benzene and dried at 100° and 20 mm of Hg. 0.83 Parts of a product containing 98.0 percent of 1-aminoanthraquinone are obtained, which corresponds to a yield of 95.1 percent of the theory. By concentrating the mother liquor, a further 0.05 parts of a product containing 71 percent of 1-aminoanthraquinone is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931253
Source datasetuspto-grants-1976_01
ORD IDord-bff9b82714de4398834f341e98b631df
Source noteuspto-grants-1976_01