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Synthesis of aryloxyacetamides from arylboronic acids and 2-bromoacetonitrile promoted by alkaline solutions of hydrogen peroxide

A novel and metal catalyst-free synthesis of aryloxyacetamides from the corresponding arylboronic acids and 2-bromoacetonitrile promoted by alkaline solutions of hydrogen peroxide has been developed involving an oxidation–reduction of eco-friendly H(2)O(2) with simultaneous reaction ipso-hydroxylati...

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Detalles Bibliográficos
Autores principales: Guo, Mengping, Li, Yingmin, Wen, Yongju, Shen, Xiuli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9847470/
https://www.ncbi.nlm.nih.gov/pubmed/36741167
http://dx.doi.org/10.1039/d2ra07451f
Descripción
Sumario:A novel and metal catalyst-free synthesis of aryloxyacetamides from the corresponding arylboronic acids and 2-bromoacetonitrile promoted by alkaline solutions of hydrogen peroxide has been developed involving an oxidation–reduction of eco-friendly H(2)O(2) with simultaneous reaction ipso-hydroxylation of arylboronic acid and hydration of the nitrile. This protocol is compatible with sensitive substituents attached to the arylboronic acid and provides desired products in moderate to good yields in pure water.