Summary
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1.
An accessible method was developed for the preparation of 5-ethyl-2-thiophthenecarboxylic acid, and by the decarboxylation of this 2-ethylthieno[2,3-b3thiophene, i.e., 2-ethylthiophthene, was formed in good yield.
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2.
The methods used for the preparation of benzo[b]thiophene-3-ol are not suitable for the synthesis of its thiophene analog, namely thieno[2,3-b]thiophener-3-ol.
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3.
Some new substituted sulfides of the thiophene series were synthesized.
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Here and below, by this name (thiophthene) we, like the Ring Index [1], understand the thienothiophene isomer of structure (thieno[2,3-b]thiophene.
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Gol'dfarb, Y.L., Litvinov, V.P. Investigation in the thiophthene series. Russ Chem Bull 12, 310–316 (1963). https://doi.org/10.1007/BF00846404
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DOI: https://doi.org/10.1007/BF00846404