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Reactions of 2-halo-2-(substituted-phenyl)-1,3-indandiones with anions of C-acids

P. Hrnčiar and E. Poláková

Department of Organic Chemistry, Faculty of Natural Sciences, Komenský University, 816 31 Bratislava

 

Abstract:  Reactions of 2-X-2-(Y-phenyl)-l,3-indandiones (X = Cl, Br; Y = H, p-N02 , p-CH30, m-CH30) with anions of acetylacetone, ethyl malonate nitromethane, and 2-nitropropane were carried out. It was found that the starting indandione was converted during the reaction into the anion of 2-(Y-phenyl)-l,3-indandione (I) and bis-2-(Y-phenyl)-l,3-indandione (II). The ratio of the products I and II was dependent on X, C-acid, and the solvent.

Full paper in Portable Document Format: 351a113.pdf

 

Chemical Papers 35 (1) 113–118 (1981)

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