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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442389Generated: October 30, 2026

1-Nitroanthraquinone → 1-Aminoanthraquinone

https://huagongshe.com/reaction/442389

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NitroanthraquinoneHCID 6704—
ReactantSodium SulfiteHCID 24437—
Product1-AminoanthraquinoneHCID 6710—

Reaction Steps

Crude 1-nitroanthraquinone (A) (10 parts) is treated with sodium sulfite in the same manner as in Example 2. The resultant suspension is subjected to centrifugation, and the supernatant is removed off by decantation. The residual wet cake comprising fine particles of 1-nitroanthraquinone with high purity is charged into an autoclave together with water (21 parts) and kept at 125° C. for 14 hours while introducing gaseous ammonia (7 parts) therein. When the completion of the amination is confirmed, ammonia is recovered, and the reaction mixture is cooled and filtered. The collected product is washed and dried to obtain 1-aminoanthraquinone with high purity (6.2 parts). The composition and the yield are as shown in Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04045454
Source datasetuspto-grants-1977_08
ORD IDord-b415eb63281546238427b5544857ef10
Source noteuspto-grants-1977_08