Ceria-supported ruthenium catalysts for the synthesis of indole via dehydrogenative N-heterocyclization

被引:27
作者
Shimura, Shun [1 ]
Miura, Hiroki [1 ]
Wada, Kenji [1 ]
Hosokawa, Saburo [1 ]
Yamazoe, Seiji [2 ]
Inoue, Masashi [1 ]
机构
[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
关键词
PALLADIUM-CONTAINING PEROVSKITES; MOLECULAR-OXYGEN; MIZOROKI-HECK; ALCOHOLS; OXIDATION; AMINES; NANOPARTICLES; CEO2; ACID; RU;
D O I
10.1039/c1cy00235j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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.
引用
收藏
页码:1340 / 1346
页数:7
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