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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172017Generated: October 25, 2026

2,5-Dihydroxyterephthalic acid → 4,6-Diamino-1,3-benzenediol 2,5-dihydroxyterepthalic acid

https://huagongshe.com/reaction/1172017

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Dihydroxyterephthalic acidHCID 69131—
Reactant4,6-Diaminoresorcinol DihydrochlorideHCID 2733648—
ReactantHCID 178524618HCID 178524618—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
Product4,6-Diamino-1,3-benzenediol 2,5-dihydroxyterepthalic acidHCID 131728418—

Reaction Steps

7 Parts by weight of 4,6-diamino-1,3-benzenediol dihydrochloride was dissolved in 33 parts by weight of water deaerated with nitrogen. 6.180 Parts by weight of 2,5-dihydroxyterephthalic acid was dissolved in 64 parts by weight of a 1M sodium hydroxide aqueous solution, followed by deaeration with nitrogen. The 4,6-diamino-1,3-benzenediol dihydrochloride aqueous solution was dropwise added to the 2,5-dihydroxyterephthalic acid disodium salt aqueous solution over 10 minutes to form a white precipitate of 4,6-diamino-1,3-benzenediol/2,5-dihydroxyterepthalic acid salt. In this case, the reaction temperature was maintained at 90° C. The resultant salt was recovered by filtering and dispersed in, and mixed with, 3,000 parts by weight of water deaerated with nitrogen, followed by re-filtering. Procedures of the above dispersing/mixing and filtering were repeated 3 times.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833644B2
Source datasetuspto-grants-2010_11
ORD IDord-dea1617d1fab4018b964b1ee9975a597
Source noteuspto-grants-2010_11