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Chemistry of Heterocyclic Compounds

, Volume 1, Issue 2, pp 105–109 | Cite as

Electrolytic methoxylation of halognofurans

  • G. P. Sokolov
  • S. A. Giller
Article
  • 52 Downloads

Abstract

α-Halogenofurans are electrolytically methoxylated in two ways in the presence of sulfuric acid electrolyte, methoxyl groups either adding at the 2 and 5 positions in the furan ring or replacing a ring halogen atom. The following are methoxylated: 2-bromo-, 2-iodofuran, 5-chloro-, 5-bromo-, and 5-iodofurfural, ethyl 5-bromopyromucate. Derivatives of 2, 2, 5-trimethoxy-2, 5-dihydrofuran are prepared, giving on hydrolysisβ-aldehydo- andβ-ketoacrylic acids.

Total anode polarization graphs are obtained in order to study the electrolytic methoxylation reaction mechanism.

Keywords

Ethyl Organic Chemistry Sulfuric Acid Reaction Mechanism Furan 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© The Faraday Press, Inc. 1966

Authors and Affiliations

  • G. P. Sokolov
    • 1
  • S. A. Giller
    • 1
  1. 1.Institute of Organic Synthesis AS Latvian SSRRiga

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