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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647025Generated: October 25, 2026

1-Nitroanthraquinone → 1-Nitroanthraquinone

https://huagongshe.com/reaction/647025

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NitroanthraquinoneHCID 6704—
Reactant9,10-Anthracenedione, 1,2-dinitro-HCID 42596—
Reactant2-NitroanthraquinoneHCID 3928593—
Product1-NitroanthraquinoneHCID 6704—
Product1-AminoanthraquinoneHCID 6710—

Reaction Steps

The nitroanthraquinone used was composed of 69.1% of 1-nitroanthraquinone, 0.7% of 2-nitroanthraquinone and 26.8% of dinitroanthraquinone, and the 1-aminoanthraquinone content in the effluent aminoanthraquinone dry cake was 73.6%. The reduction yield from 1-nitroanthraquinone to 1-aminoanthraquinone was 99.7%. The crystals of the aminoanthraquinones obtained in this and following Examples 2-6 are represented by FIG. 2. They had excellent filterability as tested by a rotary vacuum filter or a pressure filter and could be efficiently separated from waste water of reduction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04407756
Source datasetuspto-grants-1983_10
ORD IDord-ee67a3768129408880265cdd2bac9bce
Source noteuspto-grants-1983_10