Abstract
A method of preparing N-phenyl-3-hydroxy-1, 2, 3, 4-tetrahydroquinoline is developed, and some of its conversion products are obtained. The structures of N-phenyl-3-chloro-1, 2, 3, 4-tetrahydroquinoline and N-phenyl-1, 2, 3, 4-tetrahydroqunoline. are proved, the latter being formed by heating N-phenyl-3-hydroxy-1, 2, 3, 4-tetrahydroquinoline with concentrated hydrochloric acid.
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References
N. N. Vorozhtsov, Jr. and S. I. Kutkevichus, ZhOKh, 27, 2152, 1957.
German Patent 284291 (Fr., XII, 152).
W. Davies and W. Savige, J. Chem. Soc., 890, 1950.
N. N. Vorozhtsov, Jr. and S. I. Kutkevichus, Transactions of the Conference on the Chemistry, Technology, and Applications of Pyridine and Quinoline Derivatives [in Russian], Riga, October 1957.
N. N. Vorozhtsov, Jr. and S. I. Kutkevichus, ZhOKh, 28, 2682, 1958.
N. N. Vorozhtsov, Jr., G. G. Yakobson, and A. E. Ioffe, Author's Certificate No. 106585.
H. König and R. Huisgen, Berlin, 92, 429, 1959.
H. O. Jones and P. E. Evans, J. Chem. Soc., 99, 334, 1911; M. G. Edwards, R. E. Garrod, and H. O. Jones, J. Am. Chem. Soc., 101, 1376, 1912.
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Vorozhtsov, N.N., Kutkevichus, S.I. A study of the reaction products from epichlorohydrin and aromatic amines. Chem Heterocycl Compd 1, 248–251 (1966). https://doi.org/10.1007/BF00473601
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DOI: https://doi.org/10.1007/BF00473601