Ceria-supported ruthenium catalysts for the synthesis of indole via dehydrogenative N-heterocyclization
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Shimura, Shun
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Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, JapanKyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan
Shimura, Shun
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Miura, Hiroki
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Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, JapanKyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan
Miura, Hiroki
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Wada, Kenji
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Hosokawa, Saburo
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Yamazoe, Seiji
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Ryukoku Univ, Grad Sch Sci & Technol, Dept Mat Chem, Otsu, Shiga 5202194, JapanKyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan
Yamazoe, Seiji
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Inoue, Masashi
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Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, JapanKyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan
Inoue, Masashi
[1
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[1] Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan
[2] Ryukoku Univ, Grad Sch Sci & Technol, Dept Mat Chem, Otsu, Shiga 5202194, Japan
Simple heterogeneous Ru/CeO2 catalysts as well as Ru/ZrO2 catalysts were found to be quite effective for the selective direct synthesis of indole via intramolecular dehydrogenative N-heterocyclization of 2-(2-aminophenyl) ethanol, while catalysts supported on SiO2, Al2O3, TiO2, and MgO were less effective. Ru/CeO2 catalysts that were calcined at a relatively low temperature, 200 degrees C, showed excellent activity and gave indole in a yield over 99% by the reaction at 140 degrees C for 24 h (Ru catalyst 2.5 mol%). Spectroscopic studies of the Ru/CeO2 catalysts indicated the formation of Ru-IV-QO species on the surface, which is considered to be transformed into the catalytically-active species at the initial stage of the reaction. Hot filtration tests and an ICP-AES analysis indicated that these Ru/CeO2 catalysts act heterogeneously and that the leaching of ruthenium species into the solution is negligible. These catalysts could be recycled without a significant loss of activity, which suggests that the present oxide-supported catalysts are promising alternatives to conventional homogeneous catalysts.