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Synthesis of N,N-disubstituted aminoacetophenones

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

Reaction of p-bromoacetophenone with secondary amines affords mixtures of N,N-disubstituted p- and m-aminoacetophenones, with a predominance of the m-isomers.

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Literature cited

  1. M. P. Terpugova, I. L. Kotlyarevskii, Yu. I. Amosov, and R. N. Myasnikova, Izv. Akad. Nauk SSSR, Ser. Khim., 2808 (1975).

  2. P. Caubere and M. Hochu, Bull. Soc. Chim. France, 2854 (1969).

  3. A. Janousova, M. J. Benes, M. Janic, and J. Peska, Prepr. Int. Symp. Macromolecul., Helsinki,2, 699 (1972).

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  4. G. S. Kolesnikov, The Synthesis of Vinyl Derivatives of Aromatic and Heterocyclic Compounds [in Russian], Izd-vo AN SSSR (1960), p. 113.

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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 665–666, March, 1976.

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Terpugova, M.P., Amosov, Y.I., Kotlyarevskii, I.L. et al. Synthesis of N,N-disubstituted aminoacetophenones. Russ Chem Bull 25, 650–651 (1976). https://doi.org/10.1007/BF01106674

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  • DOI: https://doi.org/10.1007/BF01106674

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