Abstract
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 K2S2O8-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 K2S2O8-activated charcoal mixture and thiols, respectively, as an oxidant and sulfonylating precursors for the first time.
Cite
CITATION STYLE
Natarajan, P., Priya, & Chuskit, D. (2021). 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. RSC Advances, 11(26), 15573–15580. https://doi.org/10.1039/d1ra02377b
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.