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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225033Generated: October 25, 2026

1-Amino-4-hydroxyanthraquinone → 1-Amino-2-bromo-4-hydroxyanthraquinone

https://huagongshe.com/reaction/225033

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Amino-4-hydroxyanthraquinoneHCID 8323—
Reactant1-Amino-2-bromoanthraquinoneHCID 236895—
Reactant1-Amino-4-bromoanthraquinoneHCID 627326—
Solvent1-Amino-2-hydroxyanthra-9,10-quinoneHCID 3478173—
Product1-Amino-2-bromo-4-hydroxyanthraquinoneHCID 8320—

Reaction Steps

The progress of the bromination may be followed by thin layer chromatography or high pressure liquid chromatography so as to insure that the byproducts, 1-amino-2-bromoanthraquinone and 1-amino-4-bromoanthraquinone, represent less than 1% of the product mixture. This is essential, since hydroxylation of these two products results in 1-amino-2-hydroxyanthraquinone and 1-amino-4-hydroxyanthraquinone respectively. Both products are isolated along with the desired 1-amino-2-bromo-4-hydroxyanthraquinone and therefore give rise to a product with unsatisfactory quality.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04235789
Source datasetuspto-grants-1980_11
ORD IDord-323b5bf544664fefa041dc236dcb1427
Source noteuspto-grants-1980_11