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Aromatic polyfluoro-compounds. Part XLIX. Nucleophilic replacement reactions of 2,3,4,5,6-pentafluorostyrene
Journal of the Chemical Society C: Organic Pub Date : , DOI:10.1039/J39700001271
Abstract

Pentafluorostyrene reacts with sodium methoxide, methylamine, dimethylamine, and lithium anilide with replacement of the fluorine para to the vinyl group only. It is concluded that significant replacement by nucleophiles of fluorine ortho to a substituent X in C6F5X requires that X be of the type Y[double bond, length half m-dash]Z, that is, dipolar and unsaturated.

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