Abstract
4-Acrylamido-4-methyltetrahydropyran was obtained via the Ritter reaction on the basis of cyclic unsaturated ethers and acrylonitrile. This amide is not hydrolyzed in alkaline media but does add dichlorocarbene and bromine to the double bond. Dehydrobromination of the dibromo derivative leads to the corresponding amide with a triple bond.
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U. G. Ibatullin, D. Ya. Mukhametova, S. A. Vasil'eva, R. F. Talipov, L. V. Syurina, M. G. Safarov, and S. R. Rafikov, Izv. Akad. Nauk SSSR, Ser. Khim., No. 9, 2114 (1982).
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Deceased.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 461–462, April, 1985.
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Ibatullin, U.G., Mukhametova, D.Y., Makaeva, R.M. et al. Synthesis and transformations of 4-acrylamido-4-methyltetrahydropyran. Chem Heterocycl Compd 21, 381–382 (1985). https://doi.org/10.1007/BF00504393
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DOI: https://doi.org/10.1007/BF00504393