Abstract
The possibility of synthesizing dihydromuconic acid by cathodic carboxylation of 1,4-dibromobut-2-ene in the liquid CO2-aprotic solvent system was investigated. The low yield of dihydromuconic acid in this reaction was explained by the competing reductive debromodimerization and oligomerization of 1,4-dibromobut-2-ene, which lead to the predominant formation of 1,8-dibromo-2,6-octadiene and polymeric products.
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Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1637–1641, September, 1997.
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Grinberg, V.A., Koch, T.A., Mazin, V.M. et al. Electrocarboxylation of 1,4-dibromobut-2-ene in a CO2-DMF liquid mixture. Russ Chem Bull 46, 1560–1564 (1997). https://doi.org/10.1007/BF02502939
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DOI: https://doi.org/10.1007/BF02502939