Bonner Arlene, Baumann Marcus
School of Chemistry, University College Dublin, Science Centre South, Belfield, Dublin 4, Ireland D04 N2E2.
Org Process Res Dev. 2023 Sep 11;28(5):1567-1575. doi: 10.1021/acs.oprd.3c00213. eCollection 2024 May 17.
A new and highly efficient continuous flow process is presented for the synthesis of aziridines via the thermal Baldwin rearrangement. The process was initially explored using traditional batch synthesis techniques but suffered from moderate yields, long reaction times, and moderate diastereoselectivities. Here we demonstrate that the process can be greatly improved upon its transfer to continuous flow, which afforded the aziridine targets in high yields, short reaction times, and consistently high diastereoselectivities, with the high-throughput process rendering multigram quantities of product in short periods of time. In addition, flow processing extended the substrate scope including several examples that had failed in batch mode, thus demonstrating the value of this overlooked entry into valuable aziridine species.
本文介绍了一种通过热鲍德温重排合成氮丙啶的新型高效连续流工艺。该工艺最初采用传统的间歇合成技术进行探索,但产率中等、反应时间长且非对映选择性中等。在此,我们证明将该工艺转移至连续流后可得到极大改进,能够以高收率、短反应时间和始终如一的高非对映选择性得到氮丙啶目标产物,高通量工艺可在短时间内生产出数克量的产物。此外,流动过程扩展了底物范围,包括几个在间歇模式下失败的例子,从而证明了这种被忽视的制备有价值的氮丙啶类化合物方法的价值。