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Iron porphyrin-catalyzed N-trifluoroethylation of anilines with 2,2,2-trifluoroethylamine hydrochloride in aqueous solution

An iron porphyrin-catalyzed N-trifluoroethylation of anilines has been developed with 2,2,2-trifluoroethylamine hydrochloride as the fluorine source. This one-pot N–H insertion reaction is conducted via cascade diazotization/N-trifluoroethylation reactions. The developed transformation can afford a...

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Detalles Bibliográficos
Autores principales: Ren, Shuang, Xu, Guiming, Guo, Yongjia, Liu, Qiang, Guo, Cancheng
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/PMC9033960/
https://www.ncbi.nlm.nih.gov/pubmed/35479926
http://dx.doi.org/10.1039/d1ra03379d
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author Ren, Shuang
Xu, Guiming
Guo, Yongjia
Liu, Qiang
Guo, Cancheng
author_facet Ren, Shuang
Xu, Guiming
Guo, Yongjia
Liu, Qiang
Guo, Cancheng
author_sort Ren, Shuang
collection PubMed
description An iron porphyrin-catalyzed N-trifluoroethylation of anilines has been developed with 2,2,2-trifluoroethylamine hydrochloride as the fluorine source. This one-pot N–H insertion reaction is conducted via cascade diazotization/N-trifluoroethylation reactions. The developed transformation can afford a wide range of N-trifluoroethylated anilines in good yields using readily available primary amines and secondary anilines as starting materials.
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spelling pubmed-90339602022-04-26 Iron porphyrin-catalyzed N-trifluoroethylation of anilines with 2,2,2-trifluoroethylamine hydrochloride in aqueous solution Ren, Shuang Xu, Guiming Guo, Yongjia Liu, Qiang Guo, Cancheng RSC Adv Chemistry An iron porphyrin-catalyzed N-trifluoroethylation of anilines has been developed with 2,2,2-trifluoroethylamine hydrochloride as the fluorine source. This one-pot N–H insertion reaction is conducted via cascade diazotization/N-trifluoroethylation reactions. The developed transformation can afford a wide range of N-trifluoroethylated anilines in good yields using readily available primary amines and secondary anilines as starting materials. The Royal Society of Chemistry 2021-06-07 /pmc/articles/PMC9033960/ /pubmed/35479926 http://dx.doi.org/10.1039/d1ra03379d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Ren, Shuang
Xu, Guiming
Guo, Yongjia
Liu, Qiang
Guo, Cancheng
Iron porphyrin-catalyzed N-trifluoroethylation of anilines with 2,2,2-trifluoroethylamine hydrochloride in aqueous solution
title Iron porphyrin-catalyzed N-trifluoroethylation of anilines with 2,2,2-trifluoroethylamine hydrochloride in aqueous solution
title_full Iron porphyrin-catalyzed N-trifluoroethylation of anilines with 2,2,2-trifluoroethylamine hydrochloride in aqueous solution
title_fullStr Iron porphyrin-catalyzed N-trifluoroethylation of anilines with 2,2,2-trifluoroethylamine hydrochloride in aqueous solution
title_full_unstemmed Iron porphyrin-catalyzed N-trifluoroethylation of anilines with 2,2,2-trifluoroethylamine hydrochloride in aqueous solution
title_short Iron porphyrin-catalyzed N-trifluoroethylation of anilines with 2,2,2-trifluoroethylamine hydrochloride in aqueous solution
title_sort iron porphyrin-catalyzed n-trifluoroethylation of anilines with 2,2,2-trifluoroethylamine hydrochloride in aqueous solution
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033960/
https://www.ncbi.nlm.nih.gov/pubmed/35479926
http://dx.doi.org/10.1039/d1ra03379d
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