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Metal-free, room temperature, acid-K(2)S(2)O(8) mediated method for the nitration of olefins: an easy approach for the synthesis of nitroolefins

Here, we have developed a simple, room temperature method for the nitration of olefins by using inexpensive sodium nitrite as a source of nitro groups in the presence of trifluoroacetic acid (TFA) and potassium persulfate (K(2)S(2)O(8)) under an open atmosphere. Styrenes and mono-substituted olefins...

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Detalles Bibliográficos
Autores principales: Ambala, Srinivas, Singh, Rohit, Singh, Maninder, Cham, Pankaj Singh, Gupta, Ria, Munagala, Gurunadham, Yempalla, Kushalava Reddy, Vishwakarma, Ram A., Singh, Parvinder Pal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072150/
https://www.ncbi.nlm.nih.gov/pubmed/35530202
http://dx.doi.org/10.1039/c9ra06414a
Descripción
Sumario:Here, we have developed a simple, room temperature method for the nitration of olefins by using inexpensive sodium nitrite as a source of nitro groups in the presence of trifluoroacetic acid (TFA) and potassium persulfate (K(2)S(2)O(8)) under an open atmosphere. Styrenes and mono-substituted olefins give stereo-selective corresponding E-nitroolefins under optimized conditions, however, 1,1-bisubstituted olefins give a mixture of E- and Z-nitroolefins. The optimized conditions work well with electron-donating, electron-withdrawing, un-substituted and heterocyclic styrenes and mono-substituted olefins and give corresponding nitroolefins with good to excellent yields.