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Transfer hydrogenation co-processing of phenolic compounds and cyclohexanol

Alexey Aleksandrovich Philippov 1
Alexey Aleksandrovich Philippov
, 
1 Federal Research Center G. K. Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russian Federation
10.71267/mencom.7941
Published 2026-03-24
Communication , Volume 36, Issue 3, 356-358
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Philippov A. A., Mart'yanov O. N. Transfer hydrogenation co-processing of phenolic compounds and cyclohexanol // Mendeleev Communications. 2026. Vol. 36. No. 3. pp. 356-358.
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Philippov A. A., Mart'yanov O. N. Transfer hydrogenation co-processing of phenolic compounds and cyclohexanol // Mendeleev Communications. 2026. Vol. 36. No. 3. pp. 356-358.
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TY - JOUR
DO - 10.71267/mencom.7941
UR - https://mendcomm.colab.ws/publications/10.71267/mencom.7941
TI - Transfer hydrogenation co-processing of phenolic compounds and cyclohexanol
T2 - Mendeleev Communications
AU - Philippov, Alexey Aleksandrovich
AU - Mart'yanov, Oleg Nikolaevich
PY - 2026
DA - 2026/03/24
PB - Mendeleev Communications
SP - 356-358
IS - 3
VL - 36
ER -
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@article{2026_Philippov,
author = {Alexey Aleksandrovich Philippov and Oleg Nikolaevich Mart'yanov},
title = {Transfer hydrogenation co-processing of phenolic compounds and cyclohexanol},
journal = {Mendeleev Communications},
year = {2026},
volume = {36},
publisher = {Mendeleev Communications},
month = {Mar},
url = {https://mendcomm.colab.ws/publications/10.71267/mencom.7941},
number = {3},
pages = {356--358},
doi = {10.71267/mencom.7941}
}
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Philippov, Alexey Aleksandrovich, and Oleg Nikolaevich Mart'yanov. “Transfer hydrogenation co-processing of phenolic compounds and cyclohexanol.” Mendeleev Communications, vol. 36, no. 3, Mar. 2026, pp. 356-358. https://mendcomm.colab.ws/publications/10.71267/mencom.7941.
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Keywords

benzofuran
cyclohexanol
guaiacol
Ni catalysts
transfer hydrogenation
vanillin

Abstract

Combining cyclohexanol to cyclohexanone transformation with the reductive conversion of phenolic compounds presents a promising strategy for the co-processing of cyclohexanol and biomass-derived products. In this study, anisole, guaiacol, 2,3-benzofuran, and vanillin are hydrogenated at 200 and 250 ° C using cyclohexanol as a hydrogen donor, with the catalysts being Ni/γ-Al2O3 samples prepared via the deposition–precipitation method.

Funders

Russian Science Foundation
24-23-20044

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