Reaktionsgleichung
Cl[C:2]1[CH:10]=[C:9]([C:11]([OH:13])=[O:12])[C:8](Cl)=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].C([O-])([O-])=[O:16].[Na+].[Na+].CN[C@@H]1CCCC[C@H]1NC.Cl.[OH2:32]>CN[C@@H]1CCCC[C@H]1NC>[OH:32][C:2]1[CH:10]=[C:9]([C:11]([OH:13])=[O:12])[C:8]([OH:16])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5]Komponenten
Edukt 5
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 25 °C
Versuchsvorschrift
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%.
Aufarbeitung
- temperatureThe mixture was heated
- temperatureto reflux
- temperaturereflux
- waitwas continued for 30 min
- dissolutionwas dissolved
- customto give a deep purple solution
- additionThis solution was added to the stirred reaction mixture via syringe at 80° C. under nitrogen
- stirringstirred for 20 h at 80° C
- customproducing a dark yellow precipitate
- filtrationThe yellow precipitate was filtered
- washwashed with water
- customAfter drying
Quellen und Nachweise
- ORD-Eintrag
- ord-0f250410e0004f46833da877139ba2c4
- Quelldatensatz
- uspto-grants-2008_02
- Patentnummer
- US07335791B1
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