| Autor: |
Nasseri, Mohammad Ali, Alavi, Seyyedeh Ameneh, Kazemnejadi, Milad, Allahresani, Ali |
| Předmět: |
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| Zdroj: |
ChemistrySelect; 8/7/2019, Vol. 4 Issue 29, p8493-8499, 7p |
| Abstrakt: |
An efficient, simple and highly versatile method for the preparation of quinoline derivatives was developed via the Friedländer annulation reaction of 2‐aminoarylketones with carbonyl compounds using copper‐incorporated sulfated zirconium oxide (ZrO2/SO42−/Cu) as a heterogeneous recyclable nanocatalyst. The catalyst was characterized by FTIR, TG‐DTG, XRD, EDX, FE‐SEM and TEM analyses. Surface acidity of the catalyst was measured by pyridine adsorption followed by FTIR spectroscopy. The catalyst contains various Lewis‐ and Brønsted acid sites, which along with the incorporated copper, provides high to excellent yields for all compounds in water as a green solvent at room temperature for short reaction times. The catalyst could be efficiently reused for several runs without any appreciable loss of activity. In addition, the scalability of the process was investigated in this work. Finally, a plausible reaction mechanism was suggested for this transformation. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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