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利用芳基硝基甲烷和均相布朗斯特酸碱催化剂循环开发间歇流对映选择性氮杂亨利反应。

Development of an Intermittent-Flow Enantioselective Aza-Henry Reaction Using an Arylnitromethane and Homogeneous Brønsted Acid-Base Catalyst with Recycle.

作者信息

Tsukanov Sergey V, Johnson Martin D, May Scott A, Rosemeyer Morgan, Watkins Michael A, Kolis Stanley P, Yates Matthew H, Johnston Jeffrey N

机构信息

Small Molecule Design and Development, Eli Lilly and Company, Indianapolis, Indiana 46285, Unites States; Department of Chemistry and Vanderbilt Institute of Chemical Biology, Vanderbilt University, Nashville, Tennessee 37235, United States.

Small Molecule Design and Development, Eli Lilly and Company, Indianapolis, Indiana 46285, Unites States.

出版信息

Org Process Res Dev. 2016 Feb 19;20(2):215-226. doi: 10.1021/acs.oprd.5b00245. Epub 2016 Feb 1.

Abstract

A stereoselective aza-Henry reaction between an arylnitromethane and Boc-protected aryl aldimine using a homogeneous Brønsted acid-base catalyst was translated from batch format to an automated intermittent-flow process. This work demonstrates the advantages of a novel intermittent-flow setup with product crystallization and slow reagent addition which is not amenable to the standard continuous equipment: plug flow tube reactor (PFR) or continuous stirred tank reactor (CSTR). A significant benefit of this strategy was the integration of an organocatalytic enantioselective reaction with straightforward product separation, including recycle of the catalyst, resulting in increased intensity of the process by maintaining high catalyst concentration in the reactor. A continuous campaign confirmed that these conditions could effectively provide high throughput of material using an automated system while maintaining high selectivity, thereby addressing nitroalkane safety and minimizing catalyst usage.

摘要

使用均相布朗斯特酸碱催化剂,将芳基硝基甲烷与Boc保护的芳基醛亚胺之间的立体选择性氮杂-Henry反应从间歇式转化为自动间歇流工艺。这项工作展示了一种新型间歇流装置的优势,该装置具有产物结晶和缓慢添加试剂的特点,这是标准连续设备(活塞流管式反应器(PFR)或连续搅拌釜式反应器(CSTR))所不具备的。该策略的一个显著优点是将有机催化对映选择性反应与直接的产物分离相结合,包括催化剂的循环利用,通过在反应器中保持高催化剂浓度来提高过程强度。连续的实验证实,这些条件可以在使用自动化系统的同时有效提供高物料通量,同时保持高选择性,从而解决硝基烷烃的安全性问题并减少催化剂用量。

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J Org Chem. 2013 Nov 1;78(21):10605-16. doi: 10.1021/jo401321a. Epub 2013 Oct 15.

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