A Photochemical Protocol for the Synthesis of Weinreb and Morpholine Amides from Carboxylic Acids

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Abstract

In recent years, the development of light-mediated methods for synthetic applications has attracted high interest, because such methods constitute alternative approaches for the production of valuable chemical products. We study herein a photochemical protocol for the synthesis of Weinreb amides and morpholine amides from carboxylic acids. Various carboxylic acids were directly coupled to N,O-dimethylhydroxylamine, upon irradiation with either LED 370 nm or sunlight in the presence of 4-dimethylaminopyridine and bromotrichloromethane, providing Weinreb amides in moderate to high yields. Similarly, morpholine amides were obtained in satisfactory to high yields under sunlight or LED 370 nm irradiation. Thus, the versatile building blocks Weinreb amides and morpholine amides may be efficiently synthesized directly from carboxylic acids by light-mediated approaches, without the need of coupling reagents or pre-activation of carboxylic acids.

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Bourboula, A., Mountanea, O. G., Krasakis, G., Mantzourani, C., Kokotou, M. G., Kokotos, C. G., & Kokotos, G. (2023). A Photochemical Protocol for the Synthesis of Weinreb and Morpholine Amides from Carboxylic Acids. European Journal of Organic Chemistry, 26(24). https://doi.org/10.1002/ejoc.202300008

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