1-Naphthol Synthesis through Base-Promoted SNAr Reactions of ortho-Haloacetophenones Followed by Lewis-Acid-Catalyzed Cyclization

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Abstract

An efficient method was developed for the synthesis of 1-naphthols through NaOtBu-promoted SNAr reaction of ortho-haloacetophenones followed by Lewis acid CuI-catalyzed intramolecular condensation and isomerization. 1-Naphthol derivatives were obtained in satisfactory yields from aryl bromide and aryl iodide substrates.

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Yu, X., Zhu, P., Bao, M., Yamamoto, Y., Almansour, A. I., Arumugam, N., & Kumar, R. S. (2016). 1-Naphthol Synthesis through Base-Promoted SNAr Reactions of ortho-Haloacetophenones Followed by Lewis-Acid-Catalyzed Cyclization. Asian Journal of Organic Chemistry, 5(5), 699–704. https://doi.org/10.1002/ajoc.201600026

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