Abstract
Heating N-phenyl-2-naphthylamine with epichlorohydrin gives N-phenyl-N-(3-chloro-2-hydroxypropyl)-2-naphthylamine, which is subsequently converted to 4-phenyl-2-hydroxy-1,2,3,4-tetrahydrobenzo[f]quinoline. The latter readily loses a molecule of water.
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S. I. Kutkevichus and V. A. Darashkaite, Khim. Geterotsikl. Soedin., 1224 (1972).
S. I. Kutkevichus and N. N. Vorozhtsov, Jr., Khim. Geterotsikl. Soedin., 549 (1965).
N. N. Vorozhtsov, Jr., and S. I. Kutkevichus, Khim. Geterotsikl. Soedin., 374 (1965).
G. G. Yakobson, A. É. Ioffe, and N. N. Vorozhtsov, Jr., Izv. Sibirsk. Otd. Akad. Nauk SSSR, Ser. Khim., 156 (1963).
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See [1] for communication XV.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1228–1231, September, 1972.
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Kutkevichus, S.I., Milukas, B.I. & Samarskis, E.A. Investigation of the products of the reaction of epichlorohydrin with aromatic amines. Chem Heterocycl Compd 8, 1110–1113 (1972). https://doi.org/10.1007/BF00944225
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DOI: https://doi.org/10.1007/BF00944225