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Hydrogenation of nitroarenes on silica-supported copper catalyst

Elena Vladimirovna Shuvalova 1
Elena Vladimirovna Shuvalova
Olga Alekseevna Kirichenko 1
Olga Alekseevna Kirichenko
Published 2021-11-08
CommunicationVolume 31, Issue 6, 875-877
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Shuvalova E. V., Kirichenko O. A. Hydrogenation of nitroarenes on silica-supported copper catalyst // Mendeleev Communications. 2021. Vol. 31. No. 6. pp. 875-877.
GOST all authors (up to 50) Copy
Shuvalova E. V., Kirichenko O. A. Hydrogenation of nitroarenes on silica-supported copper catalyst // Mendeleev Communications. 2021. Vol. 31. No. 6. pp. 875-877.
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TY - JOUR
DO - 10.1016/j.mencom.2021.11.036
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2021.11.036
TI - Hydrogenation of nitroarenes on silica-supported copper catalyst
T2 - Mendeleev Communications
AU - Shuvalova, Elena Vladimirovna
AU - Kirichenko, Olga Alekseevna
PY - 2021
DA - 2021/11/08
PB - Mendeleev Communications
SP - 875-877
IS - 6
VL - 31
ER -
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@article{2021_Shuvalova,
author = {Elena Vladimirovna Shuvalova and Olga Alekseevna Kirichenko},
title = {Hydrogenation of nitroarenes on silica-supported copper catalyst},
journal = {Mendeleev Communications},
year = {2021},
volume = {31},
publisher = {Mendeleev Communications},
month = {Nov},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2021.11.036},
number = {6},
pages = {875--877},
doi = {10.1016/j.mencom.2021.11.036}
}
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Shuvalova, Elena Vladimirovna, and Olga Alekseevna Kirichenko. “Hydrogenation of nitroarenes on silica-supported copper catalyst.” Mendeleev Communications, vol. 31, no. 6, Nov. 2021, pp. 875-877. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2021.11.036.

Keywords

anilines
copper catalysts
hydrogen
hydrogenation
nitro group
nitroarenes

Abstract

A 9% Cu/SiO2 catalyst prepared by the deposition– precipitation technique was active in the hydrogenation of substituted nitrobenzenes at 170 °C and 13 atm H2 in a batch reactor. Nitro groups were selectively reduced to NH2 groups except for the case of 5-bromo-1,3-dinitrobenzene. The selectivity of the overall process is somewhat suppressed by inevitable formation of azo compounds and traces of tars due to the reactions of the obtained amines with nitroso intermediates.

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