4.8 Article

A Palladium-Catalyzed Carbonylation Approach to Acid Chloride Synthesis

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 135, 期 45, 页码 16841-16844

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AMER CHEMICAL SOC
DOI: 10.1021/ja4098093

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  1. NSERC
  2. Canadian Foundation for Innovation (CFI)
  3. FQRNT

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We describe a new approach to acid chloride synthesis via the palladium-catalyzed carbonylation of aryl iodides. The combination of sterically encumbered phosphines ((PBu3)-Bu-t) and CO coordination has been found to facilitate the rapid carbonylation of aryl iodides into acid chlorides via reductive elimination from ((Bu3P)-Bu-t)(CO)Pd(COAr)Cl. The formation of acid chlorides can also be exploited to perform traditional aminocarbonylation reactions under exceptionally mild conditions (ambient temperature and pressure), and with a range of weakly nucleophilic substrates.

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