eHydrogenation 2.0: Pd/C-Catalysed Hydrogenation of Alkenes and Alkynes without Externally Supplied H₂
5 affiliations
- 1School of Science, Faculty of Engineering and Science
- 2University of Greenwich
- 3École Nationale Supérieure de Chimie de Mulhouse (ENSCMu)
- 4Université de Haute-Alsace
- 5Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, London, UK, W12 0BZ
Abstract
We report an electrochemically driven Pd/C-catalysed method for the exhaustive hydrogenation of alkenes and alkynes without externally supplied H2. In an undivided cell, commercially available Pd/C in EtOH converts terminal and internal unsaturated substrates under mild constant-current conditions. Standard carbon-electrode/TFA conditions and a complementary Mg-anode/Et4NBF4 protocol furnish saturated products in up to quantitative yield while tolerating alcohols, ethers, esters, amides, sulfonamides, nitriles, phosphates, heterocycles, and carbon–halogen bonds. Most alkenes react at 4 F mol-1, whereas alkynes generally require 6 F mol-1. Coupling heterogeneous catalysis with electrochemical generation of reducing equivalents provides an operationally simple alternative to conventional hydrogenation with externally supplied H2.
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BibTeX
@misc{salehzadeh2026ehydrogenation,
title = {{eHydrogenation 2.0: Pd/C-Catalysed Hydrogenation of Alkenes and Alkynes without Externally Supplied H₂}},
author = {Hamid Salehzadeh and Feba T. Pulikkottil and Romain Ogier and Jack Brennan and Zhixuan He and Kevin Lam},
howpublished = {ChemRxiv},
year = {2026},
month = sep,
doi = {10.26434/chemrxiv.15008455/v1},
url = {https://chemrxiv.org/doi/full/10.26434/chemrxiv.15008455/v1},
note = {CC BY},
}
RIS
TY - UNPB
TI - eHydrogenation 2.0: Pd/C-Catalysed Hydrogenation of Alkenes and Alkynes without Externally Supplied H₂
AU - Hamid Salehzadeh
AU - Feba T. Pulikkottil
AU - Romain Ogier
AU - Jack Brennan
AU - Zhixuan He
AU - Kevin Lam
PY - 2026
DA - 2026/09/07
PB - ChemRxiv
DO - 10.26434/chemrxiv.15008455/v1
UR - https://chemrxiv.org/doi/full/10.26434/chemrxiv.15008455/v1
AB - We report an electrochemically driven Pd/C-catalysed method for the exhaustive hydrogenation of alkenes and alkynes without externally supplied H2. In an undivided cell, commercially available Pd/C in EtOH converts terminal and internal unsaturated substrates under mild constant-current conditions. Standard carbon-electrode/TFA conditions and a complementary Mg-anode/Et4NBF4 protocol furnish saturated products in up to quantitative yield while tolerating alcohols, ethers, esters, amides, sulfonamides, nitriles, phosphates, heterocycles, and carbon–halogen bonds. Most alkenes react at 4 F mol-1, whereas alkynes generally require 6 F mol-1. Coupling heterogeneous catalysis with electrochemical generation of reducing equivalents provides an operationally simple alternative to conventional hydrogenation with externally supplied H2.
ER -