This paper describes the synthesis of diaryl ethers and sulfides by utilizing microwave
heating methodology. The methodology is shown to be rapid and efficient for the coupling
of phenols or thiophenol with electron-deficient aryl halides through a SNAr reaction. The scope of the protocol can be expanded to six-membered heterocycles
bearing a hydroxyl group as well as to the reaction of 2-pyrimidinethiol with mildly
activated aryl halides, providing heteroaryl ethers and sulfides, respectively. The
advantages of the present method include the wide substrate scope, the obviation of
metal catalysts, ease of product isolation, and high purity of products.
dielectric heating - diaryl ether - diaryl sulfide - synthesis