8-Iodo-4-methyl-2-oxo-2H-chromen-7-yl Benzenesulfonate

We report a straightforward and efficient synthesis of 4-methyl-2-oxo-2H-chromen-7-yl benzenesulfonate (3a) and 8-iodo-4-methyl-2-oxo-2H-chromen-7-yl benzenesulfonate (3b) in good yields through an O-sulfonylation reaction of 7-hydroxy-2H-chromen-2-ones 1a and 1b with benzenesulfonyl chloride 2 mediated by triethylamine in dichloromethane at ambient temperature. The aryl sulfonyl esters were characterized using spectroscopic, spectrometric, and thermal analyses.

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Publication Details

Journal
Molbank
Published
2024-08-19
DOI
https://doi.org/10.3390/m1869
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
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article

8-Iodo-4-methyl-2-oxo-2H-chromen-7-yl Benzenesulfonate

Juan‐Carlos Castillo, Mario A. Macías, Luis Pulido-Moreno, Andrés Parra-Tibocha et al.
Molbank
Sulfur-Based Synthesis Techniques
article

8-Iodo-4-methyl-2-oxo-2H-chromen-7-yl Benzenesulfonate

Juan‐Carlos Castillo, Mario A. Macías, Luis Pulido-Moreno, Andrés Parra-Tibocha, Alexander Ladino-Bejarano, Diana Becerra
article en

Abstract

We report a straightforward and efficient synthesis of 4-methyl-2-oxo-2H-chromen-7-yl benzenesulfonate (3a) and 8-iodo-4-methyl-2-oxo-2H-chromen-7-yl benzenesulfonate (3b) in good yields through an O-sulfonylation reaction of 7-hydroxy-2H-chromen-2-ones 1a and 1b with benzenesulfonyl chloride 2 mediated by triethylamine in dichloromethane at ambient temperature. The aryl sulfonyl esters were characterized using spectroscopic, spectrometric, and thermal analyses.

MolbankVol. 2024(3)
Universidad de Los Andes (CO), Pedagogical and Technological University of Colombia (CO)
Clean water and sanitation
Openalex Percentile: Top 90%
Sulfur-Based Synthesis Techniques
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