User‐friendly and Green Procedure for a Photoinduced Wohl‐Ziegler Reaction

Abstract A convenient Wohl‐Ziegler bromination protocol using NBS under visible light in standard laboratory glassware is described. The monobromination reaction is efficient and selective over a wide range of substrates. Unlike previous studies, we prove that the use of a photocatalyst is unnecessary. The proposed protocol is simple to implement and applicable at the gram scale. The reaction takes place in a few tens of minutes at room temperature and offers an alternative to the use of CCl 4 , which is conventionally used for Wohl‐Ziegler bromination. Alternative conditions of bromination by CBr 4 in the presence of a photocatalyst have also been investigated.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-03-11
DOI
https://doi.org/10.1002/ejoc.202500183
Citations
2
Primary Topic
Chemical Synthesis and Reactions
Type
article
Field-Weighted Citation Impact
1.87
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article

User‐friendly and Green Procedure for a Photoinduced Wohl‐Ziegler Reaction

Laurent Evanno, Emmanuelle Drège, Florent Edde
2 citations
European Journal of Organic Chemistry
Chemical Synthesis and Reactions
1.87
article

User‐friendly and Green Procedure for a Photoinduced Wohl‐Ziegler Reaction

Laurent Evanno, Emmanuelle Drège, Florent Edde
article en
2 citations

Abstract

Abstract A convenient Wohl‐Ziegler bromination protocol using NBS under visible light in standard laboratory glassware is described. The monobromination reaction is efficient and selective over a wide range of substrates. Unlike previous studies, we prove that the use of a photocatalyst is unnecessary. The proposed protocol is simple to implement and applicable at the gram scale. The reaction takes place in a few tens of minutes at room temperature and offers an alternative to the use of CCl 4 , which is conventionally used for Wohl‐Ziegler bromination. Alternative conditions of bromination by CBr 4 in the presence of a photocatalyst have also been investigated.

European Journal of Organic ChemistryVol. 28(18)
Université Paris-Sud (FR), Centre National de la Recherche Scientifique (FR), Université Paris-Saclay (FR)
Responsible consumption and production
Openalex Percentile: Top 17%
Chemical Synthesis and Reactions
1.87
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User‐friendly and Green Procedure for a Photoinduced Wohl‐Ziegler Reaction — Laurent Evanno, Emmanuelle Drège, et al. · European Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS