分子加氢法控制金桃金娘烯醇胺化Au/ZrO2选择性

IF 5.062
Yu. S. Demidova , E.V. Suslov , I.L. Simakova , E.S. Mozhajcev , D.V. Korchagina , K.P. Volcho , N.F. Salakhutdinov , A. Simakov , D. Yu. Murzin
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引用次数: 10

摘要

在N2/H2混合气氛(9 bar)下,以Au (3wt .%)/ZrO2为催化剂,研究了一锅桃金娘烯醇胺化反应。为了提高对目标胺的选择性,探讨了加氢的影响。加氢时间取决于桃金娘烯醇转化率和加氢温度,影响反应产物的选择性。在100℃下几乎完全转化桃金娘烯醇后加氢(1 bar)使胺的产率提高到68%,保留了桃金娘烯醇初始结构中的CC键。无论桃金娘烯醇转化水平如何,在180°C加氢都会引起CC和CN键的减少,形成两个非对映体(收率高达93%),当几乎完全转化桃金娘烯醇时加氢更倾向于形成反式异构体。结果表明,在金催化剂存在的情况下,通过调节反应条件,可以实现一锅醇胺化过程中竞争性CC和CN基团的控制加氢。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Selectivity control in one-pot myrtenol amination over Au/ZrO2 by molecular hydrogen addition

Selectivity control in one-pot myrtenol amination over Au/ZrO2 by molecular hydrogen addition

The one-pot myrtenol amination was studied over Au (3 wt.%)/ZrO2 catalyst under mixed N2/H2 atmosphere (9 bar). The effect of hydrogen addition was explored with the aim to increase selectivity to the target amines. Hydrogen addition timing depending on myrtenol conversion and hydrogenation temperature affected selectivity to the reaction products. Hydrogen addition (1 bar) after almost complete myrtenol conversion at 100 °C increased the yield to amine up to 68% preserving CC bond in the initial myrtenol structure. Hydrogen addition at 180 °C irrespective of the myrtenol conversion level provoked reduction of both CC and CN bonds with formation of two diastereomers (yield up to 93%), with trans-isomer formation being preferred when hydrogen was added at almost complete myrtenol conversion. It was shown, that in the presence of a gold catalyst controlled hydrogenation of competitive CC and CN groups can be performed during one-pot alcohol amination by regulation of the reaction conditions.

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2.8 months
期刊介绍: The Journal of Molecular Catalysis A: Chemical publishes original, rigorous, and scholarly full papers that examine the molecular and atomic aspects of catalytic activation and reaction mechanisms in homogeneous catalysis, heterogeneous catalysis (including supported organometallic catalysis), and computational catalysis.
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