Abstract
Borylative functionlization of aryl fluoride was perfomed by a transition metal-free process with sodium dispersion (SD). The reaction of 4-fluorobiphenyl with SD in the prsence of boron alkoxide (iPrOBpin) afforded the borylated product in up to 62% yield. The borylation reaction also proceeded with several aryl fluorides in good to excellent yields.



![Author ORCID: We display the ORCID iD icon alongside authors names on our website to acknowledge that the ORCiD has been authenticated when entered by the user. To view the users ORCiD record click the icon. [opens in a new tab]](https://www.cambridge.org/engage/assets/public/coe/logo/orcid.png)