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HRID 495124생성일: 2026년 10월 24일

Hydrochloric Acid → 2,5-Dihydroxyterephthalic acid

https://huagongshe.com/ko/reaction/495124

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물WaterHCID 962—
반응물Sodium CarbonateHCID 10340—
반응물1,4-Benzenedicarboxylic acid, 2,5-dichloro-HCID 83739—
반응물trans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
촉매trans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
생성물2,5-Dihydroxyterephthalic acidHCID 6913194%

반응 조건

온도25 °C

반응 단계

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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07538244B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-bed48b34cd42411db5f43db5f26e8766
출처 메모uspto-grants-2009_05