Abstract
The bromination of organic molecules has been extensively studied to date, yet there is still a demand for safe and sustainable methodologies. Hazardous reagents, selectivity, low atom economy and waste production are the most persisting problems of brominating reagents. The electrochemical oxidation of bromide to bromine is a viable strategy to reduce waste by avoiding chemical oxidants. Furthermore, thein situgeneration of reactive intermediates minimizes the risk of hazardous reagents. In this work, we investigate the electrochemical generation of bromine from hydrobromic acid in a flow electrochemical reactor. Various alkenes could be converted to their corresponding dibromides, bromohydrines, bromohydrin ethers and cyclized products in good to excellent yields.
Cite
CITATION STYLE
Seitz, J., & Wirth, T. (2021). Electrochemical bromofunctionalization of alkenes in a flow reactor. Organic and Biomolecular Chemistry, 19(31), 6892–6896. https://doi.org/10.1039/d1ob01302e
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.