Electrosynthesis of 3,3′,5,5’-Tetramethyl-2,2′-biphenol in Flow

15Citations
Citations of this article
12Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

3,3′,5,5’-Tetramethyl-2,2′-biphenol is well known as an outstanding building block for ligands in transition-metal catalysis and is therefore of particular industrial interest. The electro-organic method is a powerful, sustainable, and efficient alternative to conventional synthetic approaches to obtain symmetric and non-symmetric biphenols. Here, we report the successive scale-up of the dehydrogenative anodic homocoupling of 2,4-dimethylphenol (4) from laboratory scale to the technically relevant scale in highly modular narrow gap flow electrolysis cells. The electrosynthesis was optimized in a manner that allows it to be easily adopted to different scales such as laboratory, semitechnical and technical scale. This includes not only the synthesis itself and its optimization but also a work-up strategy of the desired biphenols for larger scale. Furthermore, the challenges such as side reactions, heat development and gas evolution that arose during optimization are also discussed in detail. We have succeeded in obtaining yields of up to 62% of the desired biphenol.

Cite

CITATION STYLE

APA

Selt, M., Gleede, B., Franke, R., Stenglein, A., & Waldvogel, S. R. (2021). Electrosynthesis of 3,3′,5,5’-Tetramethyl-2,2′-biphenol in Flow. Journal of Flow Chemistry, 11(2), 143–162. https://doi.org/10.1007/s41981-020-00121-6

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free