Kyoto, Japan -- Just when we thought alkenes could only react with alcohol to yield ethers in the presence of strong acids, hydroalkoxylation may not go by the book this time. Organic Chemistry 101 will never be the same again, but the pharmaceutical industry may see the light.
Researchers at Kyoto University have announced the development of a new method of synthesizing dialkyl ethers . Rather than using conventional methods with strong acids -- entailing practical challenges such as with acid-sensitive functional groups -- the team has devised a protocol using three catalysts that hydroxylate alkenes quickly and cheaply.
This triple catalysis consists of cobalt, organic photoredox, and weak Brønsted acid catalysts.
"Our discovery allows us to synthesize pharmaceutically relevant and highly functional dialkyl ether skeletons in just one rapid step, using relatively inexpensive and accessible raw materials," explains lead author Hirohisa Ohmiya.
The three catalysts enable the precise control of electrons and protons to convert unactivated alkenes to the corresponding reactive carbocation equivalents in ethers under mild reaction conditions.
As a bonus, this catalysis has demonstrated its ability to freely utilize internal alkene partners other than terminal ones, making secondary and tertiary alkylation of alcohol reactants feasible.
The author adds, "We were also impressed that the valence of cobalt can fluctuate during the triple catalytic cycle to achieve valence-dependent functions."
"Our three catalysts perform their independent functions in a single flask to create value-added molecules efficiently and economically, possibly accelerating novel drug discoveries."
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The paper "A Triple Photoredox/Cobalt/Brønsted Acid Catalysis Enabling Markovnikov Hydroalkoxylation of Unactivated Alkenes" appeared on 27 April 2022 in Journal of the American Chemical Society , with doi: 10.1021/jacs.2c00527
About Kyoto University
Kyoto University is one of Japan and Asia's premier research institutions, founded in 1897 and responsible for producing numerous Nobel laureates and winners of other prestigious international prizes. A broad curriculum across the arts and sciences at both undergraduate and graduate levels is complemented by numerous research centers, as well as facilities and offices around Japan and the world. For more information please see: http://www.kyoto-u.ac.jp/en
Journal of the American Chemical Society
Experimental study
Not applicable
A Triple Photoredox/Cobalt/Brønsted Acid Catalysis Enabling Markovnikov Hydroalkoxylation of Unactivated Alkenes
27-Apr-2022
The authors declare no competing financial interest.