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Persulfate-activated charcoal mixture: an efficient oxidant for the synthesis of sulfonated benzo[d][1,3]oxazines from N-(2-vinylphenyl)amides and thiols in aqueous solution

A series of 2,4-aryl-4-((arylsulfonyl)methyl)-4H-benzo[d][1,3]oxazines in good to excellent yields have directly been obtained from N-(2-vinylphenyl)amides and thiols by employing a mixture of K(2)S(2)O(8)-activated charcoal in aqueous acetonitrile solution at 50 °C. A plausible mechanism for the re...

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Detalles Bibliográficos
Autores principales: Natarajan, Palani, Priya, Chuskit, Deachen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9029395/
https://www.ncbi.nlm.nih.gov/pubmed/35481158
http://dx.doi.org/10.1039/d1ra02377b
Descripción
Sumario:A series of 2,4-aryl-4-((arylsulfonyl)methyl)-4H-benzo[d][1,3]oxazines in good to excellent yields have directly been obtained from N-(2-vinylphenyl)amides and thiols by employing a mixture of K(2)S(2)O(8)-activated charcoal in aqueous acetonitrile solution at 50 °C. A plausible mechanism for the reaction is reported. It reveals that the reaction follows a radical pathway and the persulfate has been the oxygen source for formation of the sulfone group in the products. It is worth mentioning that this protocol utilizes an easily accessible K(2)S(2)O(8)-activated charcoal mixture and thiols, respectively, as an oxidant and sulfonylating precursors for the first time.