Platform demonstrates improved phase-transfer catalysis with benzyl chloride, suggesting enhanced automation in synthesis workflows.
We report a covalently immobilized crown ether‐based platform that enables phase‐transfer‐catalyzed S N 2 reactions under fully automated microplate conditions. This regenerable system overcomes key limitations of HT synthesis—solubility mismatches, mixing constraints, and purification demands—offering a zero‐waste solution for expanding the accessible reaction space in robotized synthetic workflows. The approach relies on silanized glass microvials bearing dibenzo‐18‐crown‐6 functionalities, providing a well‐defined catalytic interface between immiscible organic and aqueous phases. The dynamic movement of the phase boundary during orbital shaking ensures continuous reagent exchange without the need for mechanical stirring. Model transformations using benzyl chloride and alkali metal salts (KCN, NaSCN) validated the efficiency of the immobilized phase‐transfer system, showing comparable or superior yields relative to homogeneous conditions. The covalently anchored catalysts remained active over multiple cycles, demonstrating excellent stability and reusability. The results establish a generalizable strategy for integrating biphasic reactions into automated high‐throughput synthesis workflows by eliminating the need for free phase‐transfer catalysts.
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Sára Spátay (2025) studied this question.
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