Strong Hydrogen Bond Donating Solvents Accelerate the Passerini Three-Component Reaction

We report enhanced reaction rates of the Passerini reaction (P-3CR) using 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) as a cosolvent. Although alcoholic solvents typically increase the energy barrier of the rate-determining step for the P-3CR, we observed significant rate enhancements even when employing strong hydrogen bond donating (HBD) alcohols as cosolvents. This rate enhancement was observed for most aprotic organic solvents, with the exception of strong hydrogen bond accepting (HBA) solvents such as DMF. Experimental kinetic studies and DFT calculations provided a mechanistic rationale for our observations. An investigation of the substrate scope showed that this rate enhancement generally resulted in a (slight) increase of the overall yield in the P-3CR.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-04-03
DOI
https://doi.org/10.1021/acs.joc.5c00236
Primary Topic
Multicomponent Synthesis of Heterocycles
Type
article
Field-Weighted Citation Impact
0.00

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article

Strong Hydrogen Bond Donating Solvents Accelerate the Passerini Three-Component Reaction

Jan Pyschik, Thomas Hansen, Claudio Ferdeghini, Jordy M. Saya et al.
The Journal of Organic Chemistry
Multicomponent Synthesis of Heterocycles
article

Strong Hydrogen Bond Donating Solvents Accelerate the Passerini Three-Component Reaction

Jan Pyschik, Thomas Hansen, Claudio Ferdeghini, Jordy M. Saya, Prabhat Ranjan, Alexander Mitsos, Eelco Ruijter, Martien A. Würdemann, Romano V. A. Orrù, Minghui Wu
article en

Abstract

We report enhanced reaction rates of the Passerini reaction (P-3CR) using 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) as a cosolvent. Although alcoholic solvents typically increase the energy barrier of the rate-determining step for the P-3CR, we observed significant rate enhancements even when employing strong hydrogen bond donating (HBD) alcohols as cosolvents. This rate enhancement was observed for most aprotic organic solvents, with the exception of strong hydrogen bond accepting (HBA) solvents such as DMF. Experimental kinetic studies and DFT calculations provided a mechanistic rationale for our observations. An investigation of the substrate scope showed that this rate enhancement generally resulted in a (slight) increase of the overall yield in the P-3CR.

The Journal of Organic ChemistryVol. 90(14)
Maastricht University (NL), Vrije Universiteit Amsterdam (NL), RWTH Aachen University (DE)
Chinese Government Scholarship, H2020 Marie Skłodowska-Curie Actions
Openalex Percentile: Top 95%
Multicomponent Synthesis of Heterocycles
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Strong Hydrogen Bond Donating Solvents Accelerate the Passerini Three-Component Reaction — Jan Pyschik, Thomas Hansen, et al. · The Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS