Scalable Syntheses of 4-Substituted Pyridine-Diimines.

J Org Chem

Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, United States.

Published: December 2017

AI Article Synopsis

  • - A new, simple method for making pyridine-diimine (PDI) ligands is introduced, using affordable commercial materials instead of hazardous and complex reagents found in older methods.
  • - The synthesis method utilizes a Minisci reaction that combines pyruvic acid, silver nitrate, and persulfate to easily produce 4-functionalized diacetylpyridines.
  • - This approach not only simplifies the production of PDI ligands, but also allows for easy adjustments to their electronic properties, which can enhance various catalytic processes.

Article Abstract

A concise benchtop and scalable synthesis of pyridine-diimine (PDI) ligand frameworks is presented using inexpensive commercial starting materials as opposed to previous syntheses of these ligands, which have confronted long and tedious routes that employ toxic and often difficult to scale pyrophoric reagents. The streamlined synthesis is derived from the facile delivery of 4-functionalized diacetylpyridines from a Minisci reaction using pyruvic acid, silver nitrate, and persulfate. As the PDI ligand scaffold has been adopted for a range of catalytic applications, the ability to modulate the electronic properties of the ligand with facility may be useful for optimizing a variety of catalytic transformations.

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Source
http://dx.doi.org/10.1021/acs.joc.7b02571DOI Listing

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