Conclusions
The behavior of 3-substituted cyclohexanones in enamination and alkylation reactions was studied; the reaction of morpholinocyclohexen-3-one with acryloyl chloride gives 1-(cyclohexa-1',3'-dion-2'-yl)-3-propanoic acid.
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Literature cited
E. N. Aredova, V. V. Sevost'yanova, M. M. Krayushkin, S. S. Novikov, and N. F. Karpenko, Izv. Akad, Nauk SSSR, Ser. Khim.,1976, 1489.
E. R. Jones and F. Sondheimer, J. Chem. Soc.,1949, 616.
H. Brown and C. Gara, J. Am. Chem. Soc.83, 2952 (1961).
G. Stork, A. Brizzolara, H. Landesman, J. Szmuszkovicz, and R. Tarrell, J. Am. Chem. Soc.,85, 207 (1963).
G. V. Kondrat'eva, V. I. Gunar, L. F. Ovechkina, S. I. Zav'yalov, and A. I. Krotova, Izv. Akad. Nauk SSSR, Ser. Khim.,1967, 636.
P. W. Hickmott and J. R. Hargreaves, Tetrahedron,23, 3151 (1967).
I. I. Nazarov and S. I. Zav'yalov, Zh. Obshch. Khim.,25, 515 (1955).
M. Neeman and Y. Hashimoto, J. Am. Chem. Soc.,84, 2972 (1962).
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 926–928, April, 1978.
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Aredova, E.N., Krasutskii, P.A., Krayushkin, M.M. et al. Alkylation of 3-substituted cyclohexanone enamines. Russ Chem Bull 27, 801–803 (1978). https://doi.org/10.1007/BF00925312
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DOI: https://doi.org/10.1007/BF00925312