Issue 10, 1969

Orientation effects in the nitration of some 6- and 7-monosubstituted and 6,7-disubstituted quinolines

Abstract

The directive effects in the nitration under standard conditions of a series of substituted 4-chloroquinolines and 4-quinolones are discussed. 6-Methyl and 6-methoxy-substituents direct the nitronium ion into the 5-position whereas a 7-chloro-substituent directs this ion into the 8-position.

Article information

Article type
Paper

J. Chem. Soc. C, 1969, 1369-1372

Orientation effects in the nitration of some 6- and 7-monosubstituted and 6,7-disubstituted quinolines

N. D. Heindel, C. J. Ohnmacht, J. Molnar and P. D. Kennewell, J. Chem. Soc. C, 1969, 1369 DOI: 10.1039/J39690001369

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