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ISSN print edition: 0366-6352
ISSN electronic edition: 1336-9075
Registr. No.: MK SR 9/7
Published monthly
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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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