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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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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. |
format | Online Article Text |
id | pubmed-9033960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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