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Aminomethylation and azo-coupling reactions of 5-benzyl-3-hydroxypyridine

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

Conclusions

  1. 1.

    The aminomethylation and azo-coupling of 5-benzyl-3-hydroxypyridine take place at the 2 position of theβ-pyridinol ring.

  2. 2.

    The presence of a benzyl group in the 5 position of theβ-pyridinol ring prevents both aminomethylation and azo-coupling in the 6 position.

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Literature cited

  1. L. D. Smirnov, V. S. Zhuravlev, E. E. Merzon, B. E. Zaitsev, and K. M. Dyumaev, Khim. Geterotsikl. Soedin., 518 (1973).

  2. L. D. Smirnov, V. P. Lezina, and K. M. Dyumaev, Izv. Akad. Nauk SSSR, Ser. Khim., 198 (1965).

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Authors and Affiliations

  1. Institute of Chemical Physics, Academy of Sciences of the USSR, USSR

    L. D. Smirnov, V. S. Zhuravlev, V. P. Lezina, B. E. Zaitsev & K. M. Dyumaev

Authors
  1. L. D. Smirnov
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  2. V. S. Zhuravlev
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  3. V. P. Lezina
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  4. B. E. Zaitsev
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  5. K. M. Dyumaev
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Additional information

Translated from Izvestiya Akademii Nauk $SSR, Seriya Khimicheskaya, No. 12, pp. 2801–2803, December, 1973.

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Smirnov, L.D., Zhuravlev, V.S., Lezina, V.P. et al. Aminomethylation and azo-coupling reactions of 5-benzyl-3-hydroxypyridine. Russ Chem Bull 22, 2737–2738 (1973). https://doi.org/10.1007/BF00926154

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  • DOI: https://doi.org/10.1007/BF00926154

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