连续流动条件下异丙酚的放大和伸缩合成

IF 2 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Guilherme M. Martins, Maria F. A. Magalhães, Timothy J. Brocksom, Vanderlei S. Bagnato, Kleber T. de Oliveira
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引用次数: 1

摘要

在此,我们报告了一种机器辅助和大规模合成异丙酚的方法,异丙酚是一种用于程序镇静的短效药物,在本次COVID-19大流行期间需求量很大。连续流程方案被证明是高效的,具有巨大的工业转化潜力,通过工艺强化(24小时连续实验),每天的产量可达71.6 g。我们成功地利用连续流动方法获得了5.74 g异丙酚,生产效率为23.0 g/天(连续6 h实验),证明了该方法在分离和伸缩模式下的稳稳性。在线作业也取得了实质性进展,提供了更高的安全性和更少的浪费,也与工业应用相关。总的来说,合成策略是基于低成本对羟基苯甲酸的Friedel-Crafts二异丙基化,然后是脱羧反应,得到丙泊酚的总收率高达84%,副产物的生成非常低。异丙酚3的连续流合成提出了一个两步的方案。从4-羟基苯甲酸(1)中得到异丙基化中间体2,收率高达43.8 g,停留时间为30 min,收率为85%。异丙酚3的产率为87%,产率为71.6 g,停留时间为16 min。通过过程强化演示(24小时实验)和压缩过程强化(6小时),描述了一种安全且具有成本竞争力的机器辅助协议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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 p-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 3 is presented as a two-step protocol. The isopropylated intermediate 2 was obtained from 4-hydroxybenzoic acid (1) in up 43.8 g, 85% yield and 30 min residence time. Propofol 3 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).

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来源期刊
Journal of Flow Chemistry
Journal of Flow Chemistry CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
6.40
自引率
3.70%
发文量
29
审稿时长
>12 weeks
期刊介绍: The main focus of the journal is flow chemistry in inorganic, organic, analytical and process chemistry in the academic research as well as in applied research and development in the pharmaceutical, agrochemical, fine-chemical, petro- chemical, fragrance industry.
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