Abstract
The thio Claisen rearrangement of 2-butenyl 2-benzofuryl sulfide, cyclopenten-2-yl 2-benzofuryl sulfide, 2-butenyl 2-benzothienyl sulfide, and cyclopenten-2-yl 2-benzothienyl sulfide was investigated. The rates, energies and entropies of activation of the process were calculated, and the effect of the structure of the sulfide, the polarity of the solvent, and the temperature was demonstrated by comparison of these values. The 1,3-thioallyl rearrangement of 1-methylallyl 3-methyl-2-benzothienyl sulfide was studied, and it was shown that this reaction competes with the thio Claisen rearrangement.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1338–1341, October, 1982.
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Anisimov, A.V., Babaitsev, V.S., Kolosova, T.A. et al. Sigmatropic rearrangements of alkenyl benzofuryl and benzothienyl sulfides. Chem Heterocycl Compd 18, 1032–1036 (1982). https://doi.org/10.1007/BF00503186
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DOI: https://doi.org/10.1007/BF00503186