Polycyclic fluoroaromatic compounds. Part V. Some reactions of 1,2,3,4-tetrafluoronaphthalene

Abstract
1,2,3,4-Tetrafluoronaphthalene undergoes nucleophilic and electrophilic substitutions in the fluorocarbon and in the hydrocarbon ring respectively. On treatment with sodium methoxide, hydrazine, and lithium aluminium hydride, the 2-fluorine atom is displaced predominantly. Bromination and nitration yield mixtures of compounds substituted α and β in the hydrocarbon ring.

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