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Rhenium-Loaded TiO2: A Highly Versatile and Chemoselective Catalyst for the Hydrogenation of Carboxylic Acid Derivatives and the N-Methylation of Amines Using H-2 and CO2

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Title: Rhenium-Loaded TiO2: A Highly Versatile and Chemoselective Catalyst for the Hydrogenation of Carboxylic Acid Derivatives and the N-Methylation of Amines Using H-2 and CO2
Authors: Toyao, Takashi Browse this author →KAKEN DB
Siddiki, S. M. A. H. Browse this author
Morita, Yoshitsugu Browse this author
Kamachi, Takashi Browse this author
Touchy, Abeda S. Browse this author
Onodera, Wataru Browse this author
Kon, Kenichi Browse this author
Furukawa, Shinya Browse this author
Ariga, Hiroko Browse this author →KAKEN DB
Asakura, Kiyotaka Browse this author →KAKEN DB
Yoshizawa, Kazunari Browse this author
Shimizu, Ken-ichi Browse this author →KAKEN DB
Keywords: chemoselectivity
heterogeneous catalysis
hydrogenation
N-methylation
rhenium
Issue Date: 20-Oct-2017
Publisher: Wiley-Blackwell
Journal Title: Chemistry-A European journal
Volume: 23
Issue: 59
Start Page: 14848
End Page: 14859
Publisher DOI: 10.1002/chem.201702801
PMID: 28815903
Abstract: Herein, we report a heterogeneous TiO2-supported Re catalyst (Re/TiO2) that promotes various selective hydrogenation reactions, which includes the hydrogenation of esters to alcohols, the hydrogenation of amides to amines, and the N-methylation of amines, by using H-2 and CO2. Initially, Re/TiO2 was evaluated in the context of the selective hydrogenation of 3-phenylpropionic acid methyl ester to afford 3-phenylpropanol (p(H2)=5 MPa, T=180 degrees C), which revealed a superior performance over other catalysts that we tested in this study. In contrast to other typical heterogeneous catalysts, hydrogenation reactions with Re/TiO2 did not produce dearomatized byproducts. DFT studies suggested that the high selectivity for the formation of alcohols in favor of the hydrogenation of aromatic rings is ascribed to the higher affinity of Re towards the COOCH3 group than to the benzene ring. Moreover, Re/TiO2 showed a wide substrate scope for the hydrogenation reaction (19 examples). Subsequently, this Re/TiO2 catalyst was applied to the hydrogenation of amides, the N-methylation of amines, and the N-alkylation of amines with carboxylic acids or esters.
Rights: This is the peer reviewed version of the following article: T. Toyao, S. M. A. H. Siddiki, Y. Morita, T. Kamachi, A. S. Touchy, W. Onodera, K. Kon, S. Furukawa, H. Ariga, K. Asakura, K. Yoshizawa and K. Shimizu, Rhenium-Loaded TiO2: A Highly Versatile and Chemoselective Catalyst for the Hydrogenation of Carboxylic Acid Derivatives and the N-Methylation of Amines Using H2 and CO2, Chemistry: A European Journal, 23(59), pp.14848-14859, 2017, which has been published in final form at http://dx.doi.org/10.1039/c7ob01293d . This article may be used for non-commercial purposes in accordance With Wiley-VCH Terms and Conditions for Self-archiving.
Type: article (author version)
URI: http://hdl.handle.net/2115/71693
Appears in Collections:触媒科学研究所 (Institute for Catalysis) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 鳥屋尾 隆

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