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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442388Generated: October 31, 2026

1-Nitroanthraquinone → 1-Aminoanthraquinone

https://huagongshe.com/reaction/442388

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NitroanthraquinoneHCID 6704—
ReactantSodium SulfideHCID 14804—
ReactantSodium SulfiteHCID 24437—
Product1-AminoanthraquinoneHCID 6710—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of a wet cake of crude 1-nitroanthraquinone (A) (solid content, 28.6 %) (35 parts) and a naphthalenesulfonic acid salt-formalin condensation product (1 part) is finely pulverized by the aid of a wet type pulverizer using stainless steel balls (3 mmφ). The resultant finely pulverized wet cake (36 parts) is charged into a reaction vessel, a 10.8 % aqueous solution of sodium sulfite (28 parts) is added thereto, and the mixture is stirred at 100° C. for 9 hours. After the mixture is cooled to 45° C., sodium sulfide flakes (purity, 60 %) (9.4 parts) are added, and the mixture is treated in the same manner as in Example 7 to obtain 1-aminoanthraquinone with high purity (6.3 parts). The composition is as shown in Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04045454
Source datasetuspto-grants-1977_08
ORD IDord-42a1886da5a2490d9a75ef5d8f83e94f
Source noteuspto-grants-1977_08