The ability to parallelize reactors in reaction analysis is crucial, as it enables the rapid assessment of critical reaction conditions, such as temperature, which directly impact both the rate and selectivity of chemical reactions. In nucleophilic aromatic substitution (SNAr) reactions, where a nucleophile replaces a leaving group on an electron-deficient aromatic ring, parallel reactor setups allow for the simultaneous evaluation of multiple conditions. This facilitates the quick collection of reliable data, providing deeper insights into the reaction’s behavior and enabling the determination of key kinetic parameters, such as activation energy and reaction order. This accelerated approach is invaluable for optimizing industrial processes.
The ReactALL™ system is well-suited for simultaneously assessing the impact of reaction conditions across chemical reactions, offering independent temperature control across five reactors. In this application note, we highlight the work of Hawkins et al.[1], where they leveraged the parallelization and automated sampling features of the ReactALL to gain mechanistic insight into a model nucleophilic aromatic substitution reaction.
References:
Hawkins, J. M., Pfisterer, D. M., Algera, R. F., & Monfette, S. (2024). The ReactALL Platform: Experimental Data and Case Studies. Organic Process Research & Development. https://doi.org/10.1021/acs.oprd.4c00210