Chalcogenylation of Naphthalene Derivatives Catalyzed by Iron(III) Chloride and Potassium Iodide

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Abstract

We have developed an efficient chalcogenylation of electron-rich naphthalene derivatives catalyzed by FeCl 3and KI. The methodology provides access to several nonsymmetrical diorganoyl chalcogenides (S, Se) by selective C1 chalcogenylation of 2-naphthols or 2-naphthylamines using simple and cheap catalysts. Several control experiments supported the hypothesis that a redox reaction between Fe(III) and KI produces I 2, which catalyzed the chalcogenylation.

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Seckler, D., Da Luz, E. Q. D., Silvério, G. L., Badshah, G., Lima, D. B., Abreu, E. A., … Rampon, D. S. (2021). Chalcogenylation of Naphthalene Derivatives Catalyzed by Iron(III) Chloride and Potassium Iodide. Synlett, 32(9), 940–946. https://doi.org/10.1055/s-0040-1706748

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