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Thiele acetylation of quinones. Part II. p-Benzoquinones with halogen substituents
Journal of the Chemical Society C: Organic Pub Date : , DOI:10.1039/J39690001350
Abstract

Thiele acetylation of all mono-, di-, and tri-bromo-p-benzoquinones, and of iodo- and 2,6-di-iodo-p-benzoquinone is described. Contrary to a previous report, 2,6-dichloro-p-benzoquinone readily undergoes Thiele acetylation. The assignments of orientation of some previously reported dibromotrimethoxy-benzenes have been shown to be erroneous.

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