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使用可重复使用的二氧化锆负载氧化钨固体催化剂将苯胺选择性单烯丙基化为烯丙基苯胺。

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

作者信息

Kon Yoshihiro, Tsurumi Shota, Yamada Shunsuke, Yokoi Toshiyuki, Fujitani Tadahiro

机构信息

Interdisciplinary Research Center for Catalytic Chemistry, National Institute of Advanced Industrial Science and Technology (AIST) 1-1-1 Higashi Tsukuba Ibaraki 305-8565 Japan

Nanospace Catalysis Unit, Institute of Innovative Research, Tokyo Institute of Technology 4259 Nagatsuta Midori-ku Yokohama 226-8503 Japan.

出版信息

RSC Adv. 2022 Apr 19;12(19):11877-11884. doi: 10.1039/d2ra00198e. eCollection 2022 Apr 13.

Abstract

The monoallylation of aniline to give -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/ZrO catalyzed monoallylation process of aniline to give -allyl anilines in good yields with excellent selectivity, which enables the continuous selective flow syntheses of -allyl aniline with 97-99% selectivity. The performed detailed study about the catalytic mechanism suggests that the dispersed WO with the preservation of the W(vi) oxidation state of 10 wt% WO/ZrO with appropriate acidity and basicity is crucial for the monoallylation. The inhibition of the over allylation of the -allyl anilines is explained by the unwilling contact of the -allyl aniline with the active sites of WO/ZrO due to the steric hindrance.

摘要

苯胺的单烯丙基化反应生成烯丙基苯胺是一个基础的转化过程,能得到各种有价值的烯丙基化合物结构单元,可用于制药和电子材料生产。几十年来,可持续合成备受关注,使用烯丙醇作为烯丙基源可实现可持续性,因为通过脱水单烯丙基化反应仅生成水作为副产物。尽管使用均相金属络合物催化剂是加速脱水单烯丙基化反应的直接选择,但可溶性催化剂往往会污染产物。在此,我们展示了一种由10 wt% WO/ZrO催化的苯胺单烯丙基化反应过程,该反应能以良好的产率和优异的选择性生成烯丙基苯胺,可实现烯丙基苯胺的连续选择性流动合成,选择性达97 - 99%。对催化机理的详细研究表明,10 wt% WO/ZrO中具有适当酸度和碱度且保持W(Ⅵ)氧化态的分散态WO对单烯丙基化反应至关重要。烯丙基苯胺过度烯丙基化的抑制作用可解释为,由于空间位阻,烯丙基苯胺不愿与WO/ZrO的活性位点接触。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0011/9016830/f9001f329896/d2ra00198e-f1.jpg

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