Abstract
3-Trifluoroacetyl indoles are formed by the action of trifluoroacetic acid on indole-2-carboxylic acid and its benzo-substituted derivatives. When unsubstituted indole is refluxed with trifluoroacetic acid, it gives 3-trifluoroacetylindole in 30% yield.
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V. A. Budylin, A. N. Kost, and E. D. Matveeva, Khim. Geterotsikl. Soedin., No. 1, 55 (1972).
V. A. Budylin, A. N. Kost, E. D. Matveeva, and V. I. Minkin, Khim. Geterotsikl. Soedin., No. 1, 68 (1972).
V. A. Budylin, E. D. Matveeva, and A. N. Kost, Khim. Geterotsikl. Soedin., No. 9, 1235 (1980).
A. S. Katner, Org. Prep. Proc., 2, 297 (1970).
W. J. Houlighan (editor), Indoles, Part 1, Wiley-Interscience, New York (1972), p. 208.
W. A. Sheppard and C. M. Sharts, The Organic Chemistry of Fluorine [Russian translation], Mir, Moscow (1972), p. 307.
J. Bergman, J. Heterocycl. Chem., 7, 1071 (1970).
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Deceased.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1233–1235, September, 1981.
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Kost, A.N., Budylin, V.A., Romanova, N.N. et al. Reaction of indoles with trifluoroacetic acid. Chem Heterocycl Compd 17, 921–923 (1981). https://doi.org/10.1007/BF00505598
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DOI: https://doi.org/10.1007/BF00505598