95127-08-5Relevant articles and documents
Cross-coupling of organoboronic acids and sulfinate salts using catalytic copper(II) acetate and 1,10-phenanthroline: synthesis of aryl and alkenylsulfones
Huang, Fang,Batey, Robert A.
, p. 7667 - 7672 (2007)
A mild method for the preparation of aryl and alkenylsulfones from the cross-coupling reaction of organoboronic acids and sodium sulfinate salts is described. Optimized conditions utilize a catalytic amount of copper(II) acetate monohydrate with 1,10-phenanthroline as ligand in the presence of 4 ? molecular sieves. A co-solvent mixture of dichloromethane/DMSO was used, with reactions occurring at 40 °C under an atmosphere of oxygen. Reaction at room temperature also yields sulfone product, but in lower yields. The method tolerates a variety of substituents on the organoboronic acid, including amide, aldehyde, halide and nitro functionalities, as well as ortho-substituents. In general, the reaction is found to be less efficient using arylboronic acids bearing electron-withdrawing substituents, or using aryltrifluoroborate salts.
Three diphenyl sulfones
Jeyakanthan, Jeyaraman,Velmurugan,Vam, K. Panneersel,Soriano-Garcia, Manuel,Perumal,Chandrasekaran
, p. 630 - 633 (2007/10/03)
In 2,6-dimethylphenyl 4-nitrophenyl sulfone, C14H13-NO4S, (I), 2,6-dimethylphenyl 4-methylphenyl sulfone, C15H16O2S, (II), and 2-methylphenyl phenyl sulfone, C13H12Os