72212-81-8Relevant academic research and scientific papers
One-pot syntheses of 2,6-diiododiaryl ethers from para-EWG-substituted phenols by diacetoxyiodobenzene
Zhou, De-Jun,Yin, Shu-Qiang,Fan, Yun-Chang,Wang, Qiang
, p. 5387 - 5394 (2016)
2,6-Diiododiaryl ethers are not only useful blocks to construct substituted diaryl ethers but are also characteristic drug precursors. In this research, a one-pot tandem oxidation of phenols substituted with electron-withdrawing group at the para position by excess diacetoxyiodobenzene is proven as a novel and efficient method for preparing 2,6-diiododiaryl ethers. Using this method, three new 2,6-diiododiaryl ethers, namely, methyl 3,5-diiodo-2-methoxy-4-phenoxybenzoate (2), methyl 3,5-diiodo-4-phenoxybenzoate (6), and 1-(2,6-diiodo-4-nitrophenoxy)benzene (7) were readily obtained from the corresponding phenols, and the yields were good.
A novel and convenient approach for tosyloxylation of aromatic ring of some ortho-substituted phenolic compounds using [hydroxy(tosyloxy)iodo]benzene
Prakash, Om,Kumar, Manoj,Kumar, Rajesh
experimental part, p. 5827 - 5832 (2010/09/07)
The oxidation of some substituted monohydric phenols, containing electron-withdrawing substituents at the ortho position to the phenolic group, with [hydroxy(tosyloxy)iodo]benzene (HTIB, Koser's reagent) leads to novel tosyloxylation of aromatic ring, the
