Issue 3, 2018

Fast and accurate prediction of the regioselectivity of electrophilic aromatic substitution reactions

Abstract

While computational prediction of chemical reactivity is possible it usually requires expert knowledge and there are relatively few computational tools that can be used by a bench chemist to help guide synthesis. The RegioSQM method for predicting the regioselectivity of electrophilic aromatic substitution reactions of heteroaromatic systems is presented in this paper. RegioSQM protonates all aromatic C–H carbon atoms and identifies those with the lowest free energies in chloroform using the PM3 semiempirical method as the most nucleophilic center. These positions are found to correlate qualitatively with the regiochemical outcome in a retrospective analysis of 96% of more than 525 literature examples of electrophilic aromatic halogenation reactions. The method is automated and requires only a SMILES string of the molecule of interest, which can easily be generated using chemical drawing programs such as ChemDraw. The computational cost is 1–10 minutes per molecule depending on size, using relatively modest computational resources and the method is freely available via a web server at http://www.regiosqm.org. RegioSQM should therefore be of practical use in the planning of organic synthesis.

Graphical abstract: Fast and accurate prediction of the regioselectivity of electrophilic aromatic substitution reactions

Supplementary files

Article information

Article type
Edge Article
Submitted
23 Sep 2017
Accepted
10 Nov 2017
First published
13 Nov 2017
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2018,9, 660-665

Fast and accurate prediction of the regioselectivity of electrophilic aromatic substitution reactions

J. C. Kromann, J. H. Jensen, M. Kruszyk, M. Jessing and M. Jørgensen, Chem. Sci., 2018, 9, 660 DOI: 10.1039/C7SC04156J

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements