Preparation method of totally-substituted thiophene
A fully substituted, thiophene technology, applied in organic chemistry and other directions, can solve the problems of difficult industrial large-scale production, complex reaction steps, lack of practical value, etc., and achieve the effects of simple and easy separation of reaction products, easy operation and low cost.
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Embodiment 1
[0027] Example 1 Preparation of fully substituted thiophene compound 2a
[0028] Reaction conditions: Elemental sulfur (3.0 mmol), acetylenic compound 1a (2.0 mmol), KOH (0.2 mmol) and toluene (2.0 mL) were sequentially added to the reactor, and stirred at 100° C. for 3 hours. The obtained mixture was separated by thin layer chromatography (eluent: V petroleum ether: V ethyl acetate = 20:1), the structure of the product was confirmed by NMR and IR to be fully substituted thiophene 2a, and the yield was 84%.
[0029]
Embodiment 2
[0030] Example 2 Preparation of fully substituted thiophene compound 2b
[0031] The fully substituted thiophene compound 2b was prepared from the acetylenic compound 1b, and the reaction conditions were as in Example 1. The structure of the product was confirmed to be fully substituted thiophene 2b by NMR and IR, and the yield was 88%.
[0032]
Embodiment 3
[0033] Example 3 Preparation of fully substituted thiophene compound 2c
[0034] Thiophene compound 2c was fully substituted by acetylenic compound 1c, and the reaction conditions were as in Example 1. The structure of the product was confirmed to be fully substituted thiophene 2c by NMR and IR, and the yield was 85%.
[0035]
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