Aqueous Electrophilic Aromatic Bromination using KBr and Oxone

Electrophilic aromatic bromination reactions are an important class of chemical transformations used to synthesize key intermediates and products. We report an experimental procedure for the bromination of 4-methylanisole using KBr and Oxone in water that can be completed in 40 min at room temperature. This procedure incorporates several principles of green chemistry, providing a safer alternative to the traditional method used for bromination of aromatic compounds. The crude reaction product was characterized using IR and 1H NMR.

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Publication Details

Journal
Journal of Chemical Education
Published
2025-09-25
DOI
https://doi.org/10.1021/acs.jchemed.5c00893
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
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article

Aqueous Electrophilic Aromatic Bromination using KBr and Oxone

Dell Jensen, José R. Boquín, Mary A. Hurless, Alvin A. Theccanat
Journal of Chemical Education
Oxidative Organic Chemistry Reactions
article

Aqueous Electrophilic Aromatic Bromination using KBr and Oxone

Dell Jensen, José R. Boquín, Mary A. Hurless, Alvin A. Theccanat
article en

Abstract

Electrophilic aromatic bromination reactions are an important class of chemical transformations used to synthesize key intermediates and products. We report an experimental procedure for the bromination of 4-methylanisole using KBr and Oxone in water that can be completed in 40 min at room temperature. This procedure incorporates several principles of green chemistry, providing a safer alternative to the traditional method used for bromination of aromatic compounds. The crude reaction product was characterized using IR and 1H NMR.

Journal of Chemical EducationVol. 102(10)
Augustana College (US)
Openalex Percentile: Top 80%
Oxidative Organic Chemistry Reactions
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