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Selective monoallylation of anilines to N-allyl anilines using reusable zirconium dioxide supported tungsten oxide solid catalyst

The monoallylation of aniline to give N-allyl aniline is a fundamental transformation process that results in various kinds of valuable building block allyl compounds, which can be used in the production of pharmaceuticals and electronic materials. For decades, sustainable syntheses have been gainin...

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Autores principales: Kon, Yoshihiro, Tsurumi, Shota, Yamada, Shunsuke, Yokoi, Toshiyuki, Fujitani, Tadahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016830/
https://www.ncbi.nlm.nih.gov/pubmed/35481092
http://dx.doi.org/10.1039/d2ra00198e
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author Kon, Yoshihiro
Tsurumi, Shota
Yamada, Shunsuke
Yokoi, Toshiyuki
Fujitani, Tadahiro
author_facet Kon, Yoshihiro
Tsurumi, Shota
Yamada, Shunsuke
Yokoi, Toshiyuki
Fujitani, Tadahiro
author_sort Kon, Yoshihiro
collection PubMed
description The monoallylation of aniline to give N-allyl aniline is a fundamental transformation process that results in various kinds of valuable building block allyl compounds, which can be used in the production of pharmaceuticals and electronic materials. For decades, sustainable syntheses have been gaining much attention, and the employment of allyl alcohol as an allyl source can follow the sustainability due to the formation of only water as a coproduct through dehydrative monoallylation. Although the use of homogeneous metal complex catalysts is a straightforward choice for the acceleration of dehydrative monoallylation, the use of soluble catalysts tends to contaminate products. We herein present a 10 wt% WO(3)/ZrO(2) catalyzed monoallylation process of aniline to give N-allyl anilines in good yields with excellent selectivity, which enables the continuous selective flow syntheses of N-allyl aniline with 97–99% selectivity. The performed detailed study about the catalytic mechanism suggests that the dispersed WO(3) with the preservation of the W(vi) oxidation state of 10 wt% WO(3)/ZrO(2) with appropriate acidity and basicity is crucial for the monoallylation. The inhibition of the over allylation of the N-allyl anilines is explained by the unwilling contact of the N-allyl aniline with the active sites of WO(3)/ZrO(2) due to the steric hindrance.
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spelling pubmed-90168302022-04-26 Selective monoallylation of anilines to N-allyl anilines using reusable zirconium dioxide supported tungsten oxide solid catalyst Kon, Yoshihiro Tsurumi, Shota Yamada, Shunsuke Yokoi, Toshiyuki Fujitani, Tadahiro RSC Adv Chemistry The monoallylation of aniline to give N-allyl aniline is a fundamental transformation process that results in various kinds of valuable building block allyl compounds, which can be used in the production of pharmaceuticals and electronic materials. For decades, sustainable syntheses have been gaining much attention, and the employment of allyl alcohol as an allyl source can follow the sustainability due to the formation of only water as a coproduct through dehydrative monoallylation. Although the use of homogeneous metal complex catalysts is a straightforward choice for the acceleration of dehydrative monoallylation, the use of soluble catalysts tends to contaminate products. We herein present a 10 wt% WO(3)/ZrO(2) catalyzed monoallylation process of aniline to give N-allyl anilines in good yields with excellent selectivity, which enables the continuous selective flow syntheses of N-allyl aniline with 97–99% selectivity. The performed detailed study about the catalytic mechanism suggests that the dispersed WO(3) with the preservation of the W(vi) oxidation state of 10 wt% WO(3)/ZrO(2) with appropriate acidity and basicity is crucial for the monoallylation. The inhibition of the over allylation of the N-allyl anilines is explained by the unwilling contact of the N-allyl aniline with the active sites of WO(3)/ZrO(2) due to the steric hindrance. The Royal Society of Chemistry 2022-04-19 /pmc/articles/PMC9016830/ /pubmed/35481092 http://dx.doi.org/10.1039/d2ra00198e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Kon, Yoshihiro
Tsurumi, Shota
Yamada, Shunsuke
Yokoi, Toshiyuki
Fujitani, Tadahiro
Selective monoallylation of anilines to N-allyl anilines using reusable zirconium dioxide supported tungsten oxide solid catalyst
title Selective monoallylation of anilines to N-allyl anilines using reusable zirconium dioxide supported tungsten oxide solid catalyst
title_full Selective monoallylation of anilines to N-allyl anilines using reusable zirconium dioxide supported tungsten oxide solid catalyst
title_fullStr Selective monoallylation of anilines to N-allyl anilines using reusable zirconium dioxide supported tungsten oxide solid catalyst
title_full_unstemmed Selective monoallylation of anilines to N-allyl anilines using reusable zirconium dioxide supported tungsten oxide solid catalyst
title_short Selective monoallylation of anilines to N-allyl anilines using reusable zirconium dioxide supported tungsten oxide solid catalyst
title_sort selective monoallylation of anilines to n-allyl anilines using reusable zirconium dioxide supported tungsten oxide solid catalyst
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016830/
https://www.ncbi.nlm.nih.gov/pubmed/35481092
http://dx.doi.org/10.1039/d2ra00198e
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