Transformations of 1-(2-aminophenyl)propan-2-ol to 2-methylindoline

A1 Journal article (refereed)


Internal Authors/Editors


Publication Details

List of Authors: Heidi Bernas, Yuliya S. Demidova, Atte Aho, Irina L. Simakova, Narendra Kumar, Yosra Laribi, Philippe Perrichon, Reko Leino, Dmitry Yu. Murzin
Publisher: Springer
Publication year: 2015
Journal: Catalysis Letters
Journal acronym: Catal. Lett.
Volume number: 145
Issue number: 3
Start page: 955
End page: 963
eISSN: 1572-879X


Abstract

The transformation reaction of 1-(2-aminophenyl)propan-2-ol was studied at 200°C under argon pressure. A range of catalysts was applied including carbon, titania and zeolite supported Ru, Pd, Pt, Rh, and Ir, as well as metal free zeolites. The highest conversion was obtained with H-Beta-150 and H-Beta-25 and the highest selectivity to 2-methylindoline was achieved with 0.3 % Ir–H-Beta-150 and H-Beta-25. Although the selectivity to 2-methylindole was high for all catalysts, formation of the final product 2-methylindoline only took place over the most acidic catalysts.


Last updated on 2019-17-10 at 02:58