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DOI: 10.1055/a-2741-4407
Comparing the Effects of Solvents on Organic Thermochemical Reactions
Autor*innen
This project is supported by National Natural Science Foundation of China (No. 22371129) and the First Class Discipline of Traditional Chinese Medicine “Leading Plan” Scientific Research Special Project of NJUCM (ZYXPY2024-005).
Gefördert durch: National Natural Science Foundation of China 22371129

Abstract
For centuries, it appeared that the solvent was essential for conducting chemical experiments. It is widely accepted that solvent enables reactions to occur more efficiently. However, can solvents really enhance the efficiency of chemical reactions? To address this inquiry, we conducted this study. We examined 22 classic organic chemical reactions across 7 major categories. All reactions were divided into two parallel groups. In these two groups of experiments, except for the presence or absence of solvents, all other conditions were kept identical. The 537 data show that the yield fluctuation range in these two cases is: −13% to 19%. Based on these datasets, we draw the following conclusions: 1) The presence or absence of an excess solvent exerts minimal influence on the efficiency of most organic thermochemical reactions. 2) When one of the reactants is in liquid or gaseous state, the difference in reaction efficiency between completely solvent-free and solvent conditions is not significant. 3) When the reaction rate is relatively slow under conditions where all reactants are solid and there is no solvent at all, adding one to several equivalent amount of solvent can be comparable to the efficiency under conditions of a large amount of solvent.
Keywords
Solvent effects - Green chemistry - Organic thermochemical reaction - Free radicals - Polar reactionData availability
The data supporting this article have been included as part of the ESI.†
Publikationsverlauf
Eingereicht: 14. August 2025
Angenommen nach Revision: 07. November 2025
Accepted Manuscript online:
07. November 2025
Artikel online veröffentlicht:
02. Dezember 2025
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References
- 1 Tanaka K, Toda F. Chem Rev 2000; 100: 1025-1074
- 2 Serullas. Ann Chim (Paris) 1822; 20: 165
- 3 Hantzsch A. Justus Liebigs Ann Chem 1882; 215: 1-82
- 4 Diels O, Alder K. Justus Liebigs Ann Chem 1928; 460: 98-122
- 5 Anastas P, Eghbali N. Chem Soc Rev 2010; 39: 301-312
- 6 Sanderson H, Roy K, Benfenati E, Leszczynski J. Chem Rev 2022; 122: 3637-3710
- 7 Sheldon RA. Chem Soc Rev 2012; 41: 1437-1451
- 8a James SL, Adams CJ, Bolm C. et al. Chem Soc Rev 2012; 41: 413-447
- 8b Wang G-W. Chem Soc Rev 2013; 42: 7668-7700
- 9 Lu M, Hu W, Yun L. Chin J Org Chem 1995; 15: 561-566
- 10 Strauss C. ChemMedChem 2006; 1: 158-159
- 11a Sheldon RA. Green Chem 2005; 7: 267-278
- 11b Hessel V, Tran NN, Asrami MR. et al. Green Chem 2022; 24: 410-437
- 12 Marcus RA. J Chem Phys 1956; 24: 966-978
- 13 Marcus RA. Angew Chem Int Ed 1993; 32: 1111-1121
- 14 Eberson L. Electron Transfer Reactions in Organic Chemistry. Berlin Heidelberg: Springer-Verlag; 1987
- 15 Rosokha SV, Kochi JK. Acc Chem Res 2008; 41: 641-653