Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5280906 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
The development of a general Cu-catalyzed synthesis of (hetero)aromatic nitriles from the corresponding aryl bromides and potassium hexacyanoferrate(II) is described. This novel protocol avoids the use of highly toxic alkali cyanides and precious palladium catalysts. Best results were achieved applying Cu(BF4)2·6H2O (0.1 equiv) and N,Nâ²-dimethyl ethylenediamine (DMEDA; 1.0 equiv) in N,N-dimethyl acetamide (DMAc).
Graphical abstractThe development of a novel Cu-catalyzed synthesis of (hetero)aromatic nitriles from the corresponding aryl bromides and potassium hexacyanoferrate(II) is described. This protocol avoids the use of highly toxic alkali cyanides and precious palladium catalysts.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Thomas Schareina, Alexander Zapf, Matthias Beller,