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流动条件下的无溶剂米氏-阿尔布佐夫重排反应

Solvent-Free Michaelis-Arbuzov Rearrangement under Flow Conditions.

作者信息

Jasiak Aleksandra, Mielniczak Grażyna, Owsianik Krzysztof, Koprowski Marek, Krasowska Dorota, Drabowicz Józef

机构信息

Division of Organic Chemistry , Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences , Sienkiewicza 112 , 90-363 Łódź , Poland.

Institute of Chemistry, Health and Food Sciences, The Faculty of Mathematics and Natural Sciences , Jan Długosz University in Częstochowa , Armii Krajowej 13/15 , Częstochowa 42-201 , Poland.

出版信息

J Org Chem. 2019 Mar 1;84(5):2619-2625. doi: 10.1021/acs.joc.8b03053. Epub 2019 Feb 11.

Abstract

The first solvent- and catalyst-free procedure for the Michaelis-Arbuzov reaction under flow conditions was developed. A variety of alkylphosphonic esters could be obtained using this protocol starting from the corresponding trialkyl phosphites and even catalytic amounts of alkyl halides with very short reaction times (8.33-50 min) and excellent conversions. In general, this protocol works effectively when the alkyl halide is used in catalytic amounts as low as 5-10% only if it concerns the synthesis of homo alkylphosphonates. One equivalent and an excess of alkyl halides should be used in the reaction with alkyl phosphite if the alkyl group of the selected substrates differ. Thus, it provides a sustainable, fast alternative to the existing methods for the preparation of alkylphosphonates. The isolation of the reaction products is straightforward due to the lack of solvents and a high purity of the obtained products (conv ≥ 99%), and notably, in the catalytic procedures there are only traces of alkyl halides formed after the reaction is complete. The reactions conducted using a glass microreactor chip with an internal volume of 250 μL allow the production of 1.6-1.95 g of organophosphorus esters per hour.

摘要

开发了首个在流动条件下进行米氏-阿尔布佐夫反应的无溶剂和无催化剂方法。使用该方案,从相应的亚磷酸三烷基酯出发,甚至使用催化量的卤代烃,在非常短的反应时间(8.33 - 50分钟)内且转化率优异的情况下,可获得多种烷基膦酸酯。一般来说,仅当涉及合成均相烷基膦酸酯时,该方案在卤代烃用量低至5 - 10%的催化量下能有效起作用。如果所选底物的烷基不同,在与亚磷酸烷基酯的反应中应使用一当量及过量的卤代烃。因此,它为制备烷基膦酸酯的现有方法提供了一种可持续、快速的替代方法。由于没有溶剂且所得产物纯度高(转化率≥99%),反应产物的分离很简单,值得注意的是,在催化过程中,反应完成后仅形成痕量的卤代烃。使用内部体积为250 μL的玻璃微反应器芯片进行的反应,每小时可生产1.6 - 1.95 g有机磷酸酯。

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