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在连续流动条件下对丙泊酚进行放大及缩合合成。

Scaled up and telescoped synthesis of propofol under continuous-flow conditions.

作者信息

Martins Guilherme M, Magalhães Maria F A, Brocksom Timothy J, Bagnato Vanderlei S, de Oliveira Kleber T

机构信息

Department of Chemistry, Federal University of Sao Carlos (UFSCar), São Carlos, SP 13565-905 Brazil.

Sao Carlos Institute of Physics - University of Sao Paulo (USP), São Carlos, SP Brazil.

出版信息

J Flow Chem. 2022;12(3):371-379. doi: 10.1007/s41981-022-00234-0. Epub 2022 Jul 19.

Abstract

Herein we report a machine-assisted and scaled-up synthesis of propofol, a short-acting drug used in procedural sedation, which is extensively in demand during this COVID-19 pandemic. The continuous-flow protocol proved to be efficient, with great potential for industrial translation, reaching a production up to 71.6 g per day with process intensification (24 h-continuous experiments). We have successfully telescoped a continuous flow approach obtaining 5.74 g of propofol with productivity of 23.0 g/day (6 h-continuous experiment), proving the robustness of the method in both separated and telescoped modes. Substantial progress was also achieved for the in-line workup, which provides greater safety and less waste, also relevant for industrial application. Overall, the synthetic strategy is based on the Friedel-Crafts di-isopropylation of low-cost -hydroxybenzoic acid, followed by a decarboxylation reaction, giving propofol in up to 84% overall yield and very low by-product formation. The continuous flow synthesis of propofol is presented as a two-step protocol. The isopropylated intermediate was obtained from 4-hydroxybenzoic acid () in up 43.8 g, 85% yield and 30 min residence time. Propofol was then obtained in 71.6 g, 87% yield, and 16 min residence time. A safe and cost-competitive machine-assisted protocol is described with a process intensification demonstration (24 h experiments) and a telescoped process intensification (6 h).

摘要

在此,我们报告了一种异丙酚的机器辅助放大合成方法。异丙酚是一种用于程序镇静的短效药物,在此次新冠疫情期间需求量极大。连续流动方案被证明是高效的,具有很大的工业转化潜力,通过过程强化(24小时连续实验),日产量可达71.6克。我们成功地采用了连续流动方法,以23.0克/天的生产率(6小时连续实验)获得了5.74克异丙酚,证明了该方法在分离模式和串联模式下的稳健性。在线后处理也取得了重大进展,这提供了更高的安全性和更少的浪费,对工业应用也很重要。总体而言,合成策略基于低成本的对羟基苯甲酸的傅克二异丙基化反应,随后进行脱羧反应,异丙酚的总收率高达84%,副产物形成极少。异丙酚的连续流动合成以两步方案呈现。异丙基化中间体由4-羟基苯甲酸()制得,产量为43.8克,收率85%,停留时间30分钟。然后以71.6克、87%的收率和16分钟的停留时间得到异丙酚。本文描述了一种安全且具有成本竞争力的机器辅助方案,并进行了过程强化演示(24小时实验)和串联过程强化(6小时)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f286/9295094/8295cd1e4138/41981_2022_234_Figb_HTML.jpg

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