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氧化铈-氧化锆负载的铂作为一种高效催化剂,用于在环境条件下通过肟的氢化可持续合成羟胺和伯胺。

Ceria-Zirconia-Supported Pt as an Efficient Catalyst for the Sustainable Synthesis of Hydroxylamines and Primary Amines via the Hydrogenation of Oximes Under Ambient Conditions.

作者信息

Redina Elena, Ivanova Inna, Tkachenko Olga, Kapustin Gennady, Mishin Igor, Kustov Leonid

机构信息

Laboratory of Development and Study of Polyfunctional Catalysts, N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences, 47 Leninsky Prospect, 119991 Moscow, Russia.

出版信息

Molecules. 2025 Apr 26;30(9):1926. doi: 10.3390/molecules30091926.

DOI:10.3390/molecules30091926
PMID:40363733
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12074300/
Abstract

Amines and hydroxylamines are essential compounds in the synthesis of pharmaceuticals and other functionalized molecules. However, the synthesis of primary amines and particularly hydroxylamines remains a challenging task. The most common way to obtain amines and hydroxylamines involves the reduction of substances containing C-N bonds, such as nitro compounds, nitriles, and oximes. Among these, oximes are the most readily accessible substrates easily derived from ketones and aldehydes. However, oximes are much harder to reduce compared to nitro compounds and nitriles. The catalytic heterogeneous hydrogenation of oximes often requires harsh conditions and catalysts with high precious metal loadings, while hydroxylamines are hard to be obtained by this method. In this work, we showed that Pt supported on a porous ceria-zirconia solid solution enables the selective and atom-efficient synthesis of both hydroxylamines and amines through the hydrogenation of oximes, achieving yields of up to 99% under ambient reaction conditions in a "green" THF:HO solvent system. The high activity of the 1% Pt/CeO-ZrO catalyst (TOF > 500 h) is due to low-temperature hydrogen activation on Pt nanoparticles with the formation of a hydride, Pt-H. The strong influence of electron-donating and electron-withdrawing groups on the hydrogenation of aromatic oximes implies the nucleophilic attack of hydridic hydrogen from Pt to the electrophilic carbon of protonated oximes.

摘要

胺类和羟胺类是药物及其他功能化分子合成中的重要化合物。然而,伯胺尤其是羟胺的合成仍然是一项具有挑战性的任务。获得胺类和羟胺类最常见的方法是还原含C-N键的物质,如硝基化合物、腈类和肟类。其中,肟类是最容易获得的底物,可轻易从酮类和醛类衍生而来。然而,与硝基化合物和腈类相比,肟类更难还原。肟类的催化多相氢化通常需要苛刻的条件和高贵金属负载量的催化剂,而通过这种方法很难获得羟胺类。在这项工作中,我们表明负载在多孔氧化铈-氧化锆固溶体上的铂能够通过肟类的氢化实现羟胺类和胺类的选择性及原子经济性合成,在“绿色”的四氢呋喃:水溶剂体系中,在环境反应条件下产率高达99%。1% Pt/CeO-ZrO催化剂的高活性(TOF > 500 h⁻¹)归因于铂纳米颗粒上低温氢活化并形成氢化物Pt-H。供电子基团和吸电子基团对芳香族肟类氢化的强烈影响意味着来自Pt的氢负离子对质子化肟类亲电碳的亲核进攻。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c62/12074300/d4ae914791ac/molecules-30-01926-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c62/12074300/933af96e866d/molecules-30-01926-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c62/12074300/80b5e073d85a/molecules-30-01926-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c62/12074300/1634b4c798c7/molecules-30-01926-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c62/12074300/a3546e449ac5/molecules-30-01926-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c62/12074300/0008ddd8dbc6/molecules-30-01926-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c62/12074300/fc2ab609463b/molecules-30-01926-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c62/12074300/1f52e5e1d524/molecules-30-01926-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c62/12074300/d4ae914791ac/molecules-30-01926-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c62/12074300/933af96e866d/molecules-30-01926-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c62/12074300/80b5e073d85a/molecules-30-01926-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c62/12074300/1634b4c798c7/molecules-30-01926-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c62/12074300/a3546e449ac5/molecules-30-01926-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c62/12074300/0008ddd8dbc6/molecules-30-01926-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c62/12074300/fc2ab609463b/molecules-30-01926-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c62/12074300/1f52e5e1d524/molecules-30-01926-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c62/12074300/d4ae914791ac/molecules-30-01926-sch003.jpg

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Intermolecular 1,3-Dipolar Cycloaddition Reaction of N-Carbamoyl Nitrones Generated by N-Selective Carbamoylation of Oximes with Isocyanates.肟与异氰酸酯发生N-选择性氨甲酰化反应生成的N-氨甲酰基硝酮的分子间1,3-偶极环加成反应
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