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Issue 0, 1979
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Heterocycles in organic synthesis. Part 16. The conversion of aliphatic, aromatic, and heteroaromatic primary amines into iodides

Alan R. Katritzky,  Namek F. Eweiss  and  Pai-Lin Nie 

Abstract

22 Aliphatic primary and secondary carbylamines, aliphatic unsaturated-, hydroxy- and di-amines, benzylamines, anilines, 2-pyridylamines, and thiazolylamines have been converted in 62–96%(average 84%) yield into 1-substituted-2,4,6-triphenylpyridinium iodides by 2,4,6-triphenylpyrylium iodide. Pyrolysis of these at 135–300 °C gave the iodides corresponding to the starting amines in 52–86%(average 76%) yield.

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Article type: Paper
DOI: 10.1039/P19790000433
Citation: J. Chem. Soc., Perkin Trans. 1, 1979,0, 433-435
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    Heterocycles in organic synthesis. Part 16. The conversion of aliphatic, aromatic, and heteroaromatic primary amines into iodides

    A. R. Katritzky, N. F. Eweiss and P. Nie, J. Chem. Soc., Perkin Trans. 1, 1979, 0, 433
    DOI: 10.1039/P19790000433

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