Department of Chemistry, University of Connecticut, U-3060, 55 North Eagleville Road, Storrs, CT, 06269, USA.
Corporate Strategic Research, ExxonMobil, 1545 US 22 East, Annandale, NJ, 08801, USA.
Nat Commun. 2019 Feb 8;10(1):655. doi: 10.1038/s41467-019-08619-x.
Herein we report the first example of the catalytic aerobic partial oxidation of allyl ether to its acrylate ester derivative. Many partial oxidations often need an expensive oxidant such as peroxides or other species to drive such reactions. In addition, selective generation of esters using porous catalysts has been elusive. This reaction is catalyzed by a Li ion promoted mesoporous manganese oxide (meso-MnO) under mild conditions with no precious metals, a reusable heterogeneous catalyst, and easy isolation. This process is very attractive for the oxidation of allyl ethers. We report on the catalytic activity, selectivity, and scope of the reaction. In the best cases presented, almost complete conversion of allyl ether with near complete chemo-selectivity towards acrylate ester derivatives is observed. Based on results from controlled experiments, we propose a possible reaction mechanism for the case in which N-hydroxyphthalimide (NHPI) is used in combination with trichloroacetonitrile (CClCN).
在此,我们报告了首例烯丙基醚催化有氧部分氧化为其丙烯酸酯衍生物的实例。许多部分氧化通常需要昂贵的氧化剂,如过氧化物或其他物质来推动这些反应。此外,使用多孔催化剂选择性地生成酯类一直难以实现。该反应在温和条件下由锂离子促进的介孔氧化锰(meso-MnO)催化,无需使用贵金属、可重复使用的多相催化剂和易于分离。该工艺对于烯丙基醚的氧化非常有吸引力。我们报告了反应的催化活性、选择性和范围。在所呈现的最佳情况下,观察到烯丙基醚几乎完全转化,且对丙烯酸酯衍生物具有近乎完全的化学选择性。根据对照实验的结果,我们提出了在使用 N-羟基邻苯二甲酰亚胺(NHPI)与三氯乙腈(CClCN)结合的情况下的可能反应机制。