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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277715Generated: October 26, 2026

Phenol → 1-Phenoxyanthracene-9,10-dione

https://huagongshe.com/reaction/1277715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
Reactant1-Amino-2-bromo-4-hydroxyanthraquinoneHCID 8320—
ReactantDisperse Red 60HCID 28531—
SolventPotassium HydroxideHCID 14797—
Product1-Phenoxyanthracene-9,10-dioneHCID 3550312—

Reaction Steps

Ya. B. Shteinberg and S. S. Tkachenko, Zh. Prikl. Khim. 49 (1976) 4, 904-905, describe a process for the preparation of 1-amino-2-phenoxy-4-hydroxyanthraquinone in an aqueous medium. In this process, 1-amino-2-bromo-4-hydroxyanthraquinone is reacted with phenol in aqueous potassium hydroxide solution in the presence of dispersants at 150° C. The authors claim yields of 87-90%. On repeating this process with various dispersants, we were unable to obtain a phenoxyanthraquinone derivative which could be used as a dye. In every case, the content of 1-amino-2-phenoxy-4-hydroxyanthraquinone in the products was less than 80%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04278606
Source datasetuspto-grants-1981_07
ORD IDord-b99688e19ca1420fb40923031c03e2da
Source noteuspto-grants-1981_07