Thursday, September 15, 2016

Iodobenzene Reactions


Iodobenzene is an organoiodine admixture consisting of a benzene ring commissioned with one iodine atom. It is advantageous as a constructed average in amoebic chemistry. It is a airy achromatic liquid, although age-old samples arise yellowish.
Since the C–I tape is weaker than C–Br or C–Cl, iodobenzene is added acknowledging than bromobenzene or chlorobenzene. Iodobenzene reacts readily with magnesium to anatomy the Grignard reagent, phenylmagnesium iodide. Phenylmagnesium iodide, like the boiler analog, is a constructed agnate for the phenyl anion synthon. Iodobenzene reacts with chlorine to accord the complex, iodobenzene dichloride, which is acclimated as a solid antecedent of chlorine.

Iodobenzene can aswell serve as a substrate for the Sonogashira coupling, Heck reaction, and added metal-catalyzed couplings. These reactions advance via the oxidative accession of iodobenzene.

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