Abstract

Flow chemistry has gained considerable recognition as a simple, efficient, and safe technology for the synthesis of many types of organic and inorganic molecules ranging in scope from large complex natural products to silicon nanoparticles. In this paper we describe a method that adapts flow chemistry to the synthesis of libraries of compounds using a fluorous immiscible solvent as a spacer between reactions. The methodology was validated in the synthesis of two small heterocycle containing libraries. The reactions were performed on a 0.2 mmol scale, enabling tens of milligrams of material to be generated in a single 200 μL reaction plug. The methodology allowed library synthesis in half the time of conventional microwave synthesis while maintaining similar yields. The ability to perform multiple, potentially unrelated reactions in a single run is ideal for making small quantities of many different compounds quickly and efficiently.

Highlights

  • Flow chemistry reactors have received increased attention over the last decade as flexible platforms for organic synthesis

  • The flow reactor was composed of two HPLC pumps that were each responsible for a solvent and a reagent stream, and a variable temperature flow coil

  • In this paper we have demonstrated a new method for the production of compound libraries in a continuous flow reactor using immiscible solvent spacers

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Summary

Introduction

Flow chemistry reactors have received increased attention over the last decade as flexible platforms for organic synthesis. Their modular and simple designs have been adapted to a wide range of applications, from the synthesis of small molecules [1,2] and complex natural products [3,4,5,6], to nanoparticle synthesis [7,8]. Among their many benefits are excellent heat and mass transfer. The added ability to change temperature, residence time, and relative stoichiometry quickly and during a reaction through a computer control makes flow reactor systems excellent for reaction development and library preparation

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