Sagandira Mellisa B, Sagandira Cloudius R, Watts Paul
Nelson Mandela University, PO Box 77000, Port Elizabeth 6031, South Africa.
ACS Omega. 2025 Aug 25;10(35):40020-40031. doi: 10.1021/acsomega.5c04742. eCollection 2025 Sep 9.
Herein, we showcase how continuous flow technology enables the development of time-efficient, high-yielding synthetic routes for the anesthetic drug prilocaine. Starting from toluene nitration, prilocaine was synthesized in 74% (high-performance liquid chromatography (HPLC)) overall yield with a total residence time of just 13.6 min. Continuous flow technology markedly enhanced the nitration step's selectivity, increasing it from 59% in batch to 79%. The toluidine alkylation step benefited significantly from superheating at 150 °C and enhanced mixing in the flow system, reducing the reaction time from 48 h in batch to merely 4.4 min, affording 98% yield. Additionally, we present streamlined continuous flow reaction, telescoping, and inline workup strategies.
在此,我们展示了连续流动技术如何为麻醉药物丙胺卡因开发出省时、高产的合成路线。从甲苯硝化开始,丙胺卡因的合成总收率为74%(高效液相色谱(HPLC)),总停留时间仅为13.6分钟。连续流动技术显著提高了硝化步骤的选择性,从间歇反应中的59%提高到了79%。甲苯胺烷基化步骤在150°C的过热条件和流动系统中增强的混合作用下受益匪浅,反应时间从间歇反应中的48小时缩短至仅4.4分钟,收率达到98%。此外,我们还展示了简化的连续流动反应、串联反应和在线后处理策略。