Facile Recovery and Recycling of a Soluble Dirhodium Catalyst in Asymmetric Cyclopropanation via a Catalyst-in-Bag System

IF 3.1 3区 化学 Q2 CHEMISTRY, APPLIED
UnJin Ryu, Duc Ly, Kristin Shimabukuro, Huw M. L. Davies, Christopher W. Jones
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Abstract

A catalyst-in-bag system facilitates the recovery and recycling of chiral dirhodium carboxylate catalysts used for enantioselective, intermolecular cyclopropanation. The catalyst-in-bag system incorporates a soluble enantioselective dirhodium complex catalyst within a reusable, commercial dialysis membrane. Dirhodium catalysts of different sizes are examined, and two catalysts with molecular weights above 2400 Da are well-retained by the membrane. The catalyst Rh2(S-TPPTTL)4 [TPPTTL = (1,3-dioxo-4,5,6,7-tetraphenylisoindolin-2-yl)-3,3-dimethylbutanoate] is explored in enantioselective cyclopropanation reactions under a variety of conditions. The Rh2(S-TPPTTL)4 catalyst, when contained in the catalyst-in-bag system, provides high yields and enantioselectivities, akin to the homogeneous catalyst in solution, with negligible rhodium permeation out of the bag over five catalytic cycles. The catalyst-in-bag approach facilitates recovery of the expensive rhodium metal and ligand, with only ppm level Rh detected in the reaction products. The flexible and expandable catalyst-in-bag system can be accommodated in vessels of different shapes and dimensions.

Abstract Image

通过催化剂袋系统在不对称环丙烷化过程中简便地回收和循环利用可溶性二铑催化剂
袋装催化剂系统有助于回收和循环利用用于对映选择性分子间环丙烷化的手性羧酸二氢铑催化剂。袋装催化剂系统将可溶性对映体选择性二氢铑络合物催化剂装入可重复使用的商用透析膜中。对不同大小的二铑催化剂进行了研究,其中两种分子量超过 2400 Da 的催化剂被膜很好地保留下来。研究了催化剂 Rh2(S-TPPTTL)4 [TPPTTL = (1,3-dioxo-4,5,6,7-tetraphenylisoindolin-2-yl)-3,3-dimethylbutanoate] 在各种条件下的对映体选择性环丙烷化反应。当 Rh2(S-TPPTTL)4催化剂装入催化剂袋系统中时,可提供高产率和高对映选择性,与溶液中的均相催化剂类似,在五个催化循环中,铑从催化剂袋中渗透出来的程度可以忽略不计。袋装催化剂方法有利于回收昂贵的金属铑和配体,反应产物中检测到的铑含量仅为ppm。袋装催化剂系统具有灵活性和可扩展性,可以安装在不同形状和尺寸的容器中。
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来源期刊
CiteScore
6.90
自引率
14.70%
发文量
251
审稿时长
2 months
期刊介绍: The journal Organic Process Research & Development serves as a communication tool between industrial chemists and chemists working in universities and research institutes. As such, it reports original work from the broad field of industrial process chemistry but also presents academic results that are relevant, or potentially relevant, to industrial applications. Process chemistry is the science that enables the safe, environmentally benign and ultimately economical manufacturing of organic compounds that are required in larger amounts to help address the needs of society. Consequently, the Journal encompasses every aspect of organic chemistry, including all aspects of catalysis, synthetic methodology development and synthetic strategy exploration, but also includes aspects from analytical and solid-state chemistry and chemical engineering, such as work-up tools,process safety, or flow-chemistry. The goal of development and optimization of chemical reactions and processes is their transfer to a larger scale; original work describing such studies and the actual implementation on scale is highly relevant to the journal. However, studies on new developments from either industry, research institutes or academia that have not yet been demonstrated on scale, but where an industrial utility can be expected and where the study has addressed important prerequisites for a scale-up and has given confidence into the reliability and practicality of the chemistry, also serve the mission of OPR&D as a communication tool between the different contributors to the field.
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