Journal
GREEN CHEMISTRY
Volume 16, Issue 6, Pages 3039-3044Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4gc00153b
Keywords
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Funding
- National Natural Science Foundation of China [21125314, 21021003]
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The gold-catalyzed synthesis of benzimidazoles from 2-nitroanilines and CO2 in the presence of H-2 was reported, and a series of benzimidazoles were obtained under relatively mild conditions. Several supported Au catalysts including Au/TiO2, Au/Al2O3, Au/ZnO, Au/polyurea and Au/hydrotalcite were examined for the synthesis of benzimidazole from the reaction of 2-nitroaniline with CO2 and H-2, among which Au/TiO2 displayed the best performance. The reaction mechanism was investigated, and it was found that the production of benzimidazole underwent the formation of o-phenylenediamine via the hydrogenation of 2-nitroaniline, followed by the cyclization of o-phenylenediamine with CO2 and H-2. This work provides a CO2-involved route for the synthesis of benzimidazoles, which may widen the applications of CO2 in the chemical synthesis.
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