| Literature DB >> 31895983 |
Boyoung Y Park1, Michael T Pirnot1, Stephen L Buchwald1.
Abstract
We report a visible light-mediated flow process for C-N cross-coupling of (hetero)aryl halides with a variety of amine coupling partners through the use of a photoredox/nickel dual catalyst system. Compared to the method in batch, this flow process enables a broader substrate scope, including less-activated (hetero)aryl bromides and electron-deficient (hetero)aryl chlorides, and significantly reduced reaction times (10 to 100 min). Furthermore, scale up of the reaction, demonstrated through the synthesis of tetracaine, is easily achieved, delivering the C-N cross-coupled products in consistently high yield of 84% on up to a 10 mmol scale.Entities:
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Year: 2020 PMID: 31895983 DOI: 10.1021/acs.joc.9b03107
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354