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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495124Generated: October 25, 2026

Hydrochloric Acid → 2,5-Dihydroxyterephthalic acid

https://huagongshe.com/reaction/495124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant1,4-Benzenedicarboxylic acid, 2,5-dichloro-HCID 83739—
Reactanttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
Catalysttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
Product2,5-Dihydroxyterephthalic acidHCID 6913194%

Reaction Conditions

Temperature25 °C

Reaction Steps

Under nitrogen, 2.00 g (8.51 mmol) of 2,5-dichloroterephthalic acid was combined with 10 g of H2O. 0.938 g (8.85 mmol) of Na2CO3 was then added. The mixture was heated to reflux with stirring for 30 min, remaining under a nitrogen atmosphere. Another 1.31 g (12.34 mmol) of Na2CO3 was added to the reaction mixture and reflux was continued for 30 min. Separately, 12 mg of CuBr and 24 mg of rac-trans-N,N′-dimethylcyclohexane-1,2-diamine (Ligand F) were combined with 2 mL H2O under nitrogen. The resulting mixture was stirred under an air atmosphere until the CuBr was dissolved to give a deep purple solution. This solution was added to the stirred reaction mixture via syringe at 80° C. under nitrogen and stirred for 20 h at 80° C. After cooling to 25° C., the reaction mixture was acidified with HCl (conc.), producing a dark yellow precipitate. The yellow precipitate was filtered and washed with water. After drying, a total of 1.59 g (8.03 mmol, 94% yield) 2,5-dihydroxyterephthalic acid was collected. The purity was determined by 1H NMR to be 95%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538244B2
Source datasetuspto-grants-2009_05
ORD IDord-bed48b34cd42411db5f43db5f26e8766
Source noteuspto-grants-2009_05