On May 16, 2014, Li, Yiming; Pu, Jiahua; Jiang, Xuefeng published an article.Recommanded Product: Benzyl(4-bromophenyl)sulfane The title of the article was A Highly Efficient Cu-Catalyzed S-Transfer Reaction: From Amine to Sulfide. And the article contained the following:
A highly efficient Cu-catalyzed dual C-S bonds formation reaction, proceeding in alc. and water under air, is reported, in which inodorous stable Na2S2O3 is used as a sulfurating reagent. This powerful strategy provides a practical and efficient approach to construct thioethers, using readily available aromatic amines and alkyl halides as starting materials. Sensitive and synthetic useful functional groups could be tolerated. Furthermore, pharmaceuticals, glucose, an amino acid, and a chiral ligand are successfully furnished by this late-stage sulfuration strategy. The experimental process involved the reaction of Benzyl(4-bromophenyl)sulfane(cas: 53136-21-3).Recommanded Product: Benzyl(4-bromophenyl)sulfane
The Article related to thioether preparation dual carbon sulfur bond formation copper catalyst, aromatic amine alkyl halide sulfuration sodium thiosulfate sulfurating reagent, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Phenols, Thiophenols, and Derivatives Including Phenol and Thiophenol Ethers and Esters and other aspects.Recommanded Product: Benzyl(4-bromophenyl)sulfane
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem