Alkylation of 2-, 4-, and 8-trialkylsiloxyquinolines by methyl iodide

Authors

  • Э. Лукeвиц Latvian Institute of Organic Synthesis, Riga LV-1006
  • И. Сегал Latvian Institute of Organic Synthesis, Riga LV-1006
  • И. Биргеле Latvian Institute of Organic Synthesis, Riga LV-1006
  • А. Заблоцкая Latvian Institute of Organic Synthesis, Riga LV-1006

Abstract

Trimethyl- and triethylsilyl ethers of 2-, 4-, and 8-hydroxyquinolines have been prepared. The alkylation of these siloxyquinolines by methyl iodide has been studied. In the case of 4-trimethylsiloxyquinoldine, it has been established that both N- and O-alkylation products are formed.

How to Cite
Lukevits, É.; Segal, I.; Birgele, I.; Zablotskaya, A. Chem. Heterocycl. Compd. 1994, 30, 1061. [Khim. Geterotsikl. Soedin. 1994, 1225.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01171165

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Published

1994-09-25

Issue

No. 9 (1994)

Section

Original Papers