Degrees of Sulfonation: Mapping the Reactivity Landscape of Acridine and Acridone

Although sulfonated acridines and acridones are valuable scaffolds in diagnostics and materials science, to our best knowledge, there is no comprehensive study that addresses how the degree of sulfonation depends on reaction parameters. To fill this gap, we investigated the sulfonation behavior of unsubstituted acridine and acridone under classical conditions, using sulfuric acid, oleum, and chlorosulfonic acid. A factorial experimental design was applied to systematically evaluate the influence of temperature and reagent excess on the extent of sulfonation, while keeping the reaction time constant. Products were analyzed by HPLC–MS/MS to determine the degree of sulfonation and its distribution. Regioselectivity and product isolation were not addressed in this study. Our results provide a foundational dataset for controlling sulfonation level for these heterocycles and can help future synthetic applications where defined sulfonation patterns are desired.

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Publication Details

Journal
Organics
Published
2025-09-12
DOI
https://doi.org/10.3390/org6030043
Primary Topic
Organic and Inorganic Chemical Reactions
Type
article
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article

Degrees of Sulfonation: Mapping the Reactivity Landscape of Acridine and Acridone

Ádám Golcs, Péter Huszthy, Sára Spátay, Péter Kisfaludi
Organics
Organic and Inorganic Chemical Reactions
article

Degrees of Sulfonation: Mapping the Reactivity Landscape of Acridine and Acridone

Ádám Golcs, Péter Huszthy, Sára Spátay, Péter Kisfaludi
article en

Abstract

Although sulfonated acridines and acridones are valuable scaffolds in diagnostics and materials science, to our best knowledge, there is no comprehensive study that addresses how the degree of sulfonation depends on reaction parameters. To fill this gap, we investigated the sulfonation behavior of unsubstituted acridine and acridone under classical conditions, using sulfuric acid, oleum, and chlorosulfonic acid. A factorial experimental design was applied to systematically evaluate the influence of temperature and reagent excess on the extent of sulfonation, while keeping the reaction time constant. Products were analyzed by HPLC–MS/MS to determine the degree of sulfonation and its distribution. Regioselectivity and product isolation were not addressed in this study. Our results provide a foundational dataset for controlling sulfonation level for these heterocycles and can help future synthetic applications where defined sulfonation patterns are desired.

OrganicsVol. 6(3)
Semmelweis University (HU), Budapest University of Technology and Economics (HU)
Openalex Percentile: Top 75%
Organic and Inorganic Chemical Reactions
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