Abstract
It was established that N-acetylindoxyl oxime is converted to N-acetylindoxyl acetyloxime when it is heated to 50 ° C in a mixture of acetic acid and acetic anhydride. If the reaction is carried out by refluxing, N-acetyl-2-acetoxy- 3-acetam-idoindole, which undergoes rearrangement to 1,3-diacetyl-3-acetamidooxindole when it is heated, is also formed.
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G. N. Kurilo, S. Yu. Ryabova, and A. N. Grinev, Khim. Geterotsikl. Soedin., No. 6, 832 (1979).
L. Julian and A. Magnani, J. Am. Chem. Soc., 71, 3207 (1949).
G. C. Levy and G. L. Nelson, Carbon-13 Nuclear Magnetic Resonance for Organic Chemists, New York (1972).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1068–1070, August, 1980.
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Grinev, A.N., Ryabova, S.Y., Kurilov, G.N. et al. Intramolecular rearrangement of N-acetylindoxyl oxime. Chem Heterocycl Compd 16, 828–830 (1980). https://doi.org/10.1007/BF00513164
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DOI: https://doi.org/10.1007/BF00513164