Abstract
In the presence of catalysts (Al2O3, Al2O3 activated by HCl, and 5, 10, and 20% ZnCl2/Al2O3), 2- and 3-methylbenzothiophenes undergo mutual isomerization, dealkylation, and disproportionation to benzothiophene and 2,3-dimethylbenzothiophene at 250–450°C and space velocities of 0.1 and 0.8 h−1. An ionic mechanism is proposed for the isomerization reaction.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1079–1082, August, 1977.
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Korepanov, A.N., Danilova, T.A. & Viktorova, E.A. Reactions of 2-and 3-methylbenzothiophenes in the presence of heterogeneous acid catalysts. Chem Heterocycl Compd 13, 868–871 (1977). https://doi.org/10.1007/BF00488912
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DOI: https://doi.org/10.1007/BF00488912