Using cuprous iodide as the catalyst, aryl halides reacted with phenols to form diaryl ethers. The reaction conditions were optimized: aryl halides (1 equiv) reacted with phenol (1 equiv) at 130° C in DMF for 16 h with cuprous iodide (10 mol%), cesium carbonate (2.5 equiv) as the base, and tetramethylenediamine (5 mol%) as the ligand. Under the optimum conditions, reaction conversion with time was summarized. The structural parameters of four types of ...
[Oliveira, Ana M. A. G.; Raposo, M. Manuela M.; Oliveira-Campos, Ana M. F.; Griffiths, John; Machado, Antonio E. H. Helvetica Chimica Acta, 2003 , vol. 86, # 8 p. 2900 - 2907]