Issue 13, 1969

Aryne chemistry. Part XVIII. Some reactions of tetrahalogenobenzynes with styrene and substituted styrenes

Abstract

Tetrachlorobenzyne and tetrafluorobenzyne react with styrene to yield predominantly or exclusively 1,2,3,4-tetrahalogeno-9,10-dihydrophenanthrenes or 1,2,3,4-tetrahalogenophenanthrenes in good yield. Similar reactions are reported in which the arynes were generated in the presence of α-methyl-, trans-β-methyl-, 2-methyl-, 3-methyl-, 4-methyl-, and 2,4-dimethyl-styrene. Reactions were also carried out with trans-stilbene, 1,1-diphenylethylene, 1-phenylcyclohexene, and 1-vinylnaphthalene. The mechanism of formation of 1,2,3,4-tetrafluoro-9,10-dihydrophenanthrene has been studied by use of suitably deuteriated compounds. A discussion of the mechanism of formation of 1,2,3,4-tetrafluorophenanthrene, and of 9,10-dihydro-9-phenylphenanthrene in the reaction of benzyne with styrene, is based on reactions with deuteriated styrenes.

Article information

Article type
Paper

J. Chem. Soc. C, 1969, 1684-1689

Aryne chemistry. Part XVIII. Some reactions of tetrahalogenobenzynes with styrene and substituted styrenes

R. Harrison, H. Heaney, J. M. Jablonski, K. G. Mason and J. M. Sketchley, J. Chem. Soc. C, 1969, 1684 DOI: 10.1039/J39690001684

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