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微反应器中偶氮化合物合成过程中重氮化合物的原位生成与反应淬灭

The in situ generation and reactive quench of diazonium compounds in the synthesis of azo compounds in microreactors.

作者信息

Akwi Faith M, Watts Paul

机构信息

Nelson Mandela Metropolitan University, University Way, Port Elizabeth, 6031, South Africa.

出版信息

Beilstein J Org Chem. 2016 Sep 6;12:1987-2004. doi: 10.3762/bjoc.12.186. eCollection 2016.

Abstract

In this paper, a micro-fluidic optimized process for the continuous flow synthesis of azo compounds is presented. The continuous flow synthesis of Sudan II azo dye was used as a model reaction for the study. At found optimal azo coupling reaction temperature and pH an investigation of the optimum flow rates of the reactants for the diazotization and azo coupling reactions in Little Things Factory-MS microreactors was performed. A conversion of 98% was achieved in approximately 2.4 minutes and a small library of azo compounds was thus generated under these reaction conditions from couplers with aminated or hydroxylated aromatic systems. The scaled up synthesis of these compounds in PTFE tubing (i.d. 1.5 mm) was also investigated, where good reaction conversions ranging between 66-91% were attained.

摘要

本文介绍了一种用于偶氮化合物连续流合成的微流控优化工艺。以苏丹II偶氮染料的连续流合成为模型反应进行研究。在确定的最佳偶氮偶联反应温度和pH值下,对在“小物件工厂-MS”微反应器中进行重氮化和偶氮偶联反应的反应物最佳流速进行了研究。在约2.4分钟内实现了98%的转化率,因此在这些反应条件下,由具有胺化或羟基化芳香体系的偶联剂生成了一个小型偶氮化合物库。还研究了在聚四氟乙烯管(内径1.5毫米)中这些化合物的放大合成,在此获得了66%-91%的良好反应转化率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3db/5082718/d3422541208c/Beilstein_J_Org_Chem-12-1987-g010.jpg

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