1,2‐Dibromoarylalkanes from Simple Arylalkanes. 2,3‐Dichloro‐5,6‐dicyano‐1,4‐benzoquinone‐Mediated One‐Pot Reaction

The presented reaction protocol for the bromination of arylalkanes gives the products of 1,2‐dibromination at the alkane chain. This one‐pot process is carried out under mild conditions using 2,3‐dichloro‐5,6‐dicyano‐1,4‐benzoquinone , blue light (470 nm), and a manganese catalyst based on a porphyrin skeleton. In the case of an analogous reaction carried out without adding bromine, the products oxidised at the benzylic CH position are obtained.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-08-05
DOI
https://doi.org/10.1002/ejoc.202500531
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
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article

1,2‐Dibromoarylalkanes from Simple Arylalkanes. 2,3‐Dichloro‐5,6‐dicyano‐1,4‐benzoquinone‐Mediated One‐Pot Reaction

Karolina Hurej, Audrey Pranowo, Kinga Szydełko, Dominika Elmerych
European Journal of Organic Chemistry
Oxidative Organic Chemistry Reactions
article

1,2‐Dibromoarylalkanes from Simple Arylalkanes. 2,3‐Dichloro‐5,6‐dicyano‐1,4‐benzoquinone‐Mediated One‐Pot Reaction

Karolina Hurej, Audrey Pranowo, Kinga Szydełko, Dominika Elmerych
article en

Abstract

The presented reaction protocol for the bromination of arylalkanes gives the products of 1,2‐dibromination at the alkane chain. This one‐pot process is carried out under mild conditions using 2,3‐dichloro‐5,6‐dicyano‐1,4‐benzoquinone , blue light (470 nm), and a manganese catalyst based on a porphyrin skeleton. In the case of an analogous reaction carried out without adding bromine, the products oxidised at the benzylic CH position are obtained.

European Journal of Organic Chemistry
University of Wrocław (PL)
Openalex Percentile: Top 85%
Oxidative Organic Chemistry Reactions
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