Diethyl (Bromodifluoromethyl)phosphonate is a difluorocarbene precursor. The P-C bond can be hydrolyzed by KOH at -78 °C to room temperature to generate difluorocarbene (:CF2). When using phenols as substrates, the corresponding difluoromethyl ethers can be obtained via difluoromethylation in good yields. This reaction proceeds under very mild conditions, thus, even phenols bearing enolizable groups can be difluoromethylated at their phenolic hydroxy groups.
Your session will timeout in 10 minutes. You will be redirected to the HOME page after session timeout. Please click the button to continue session from the same page. minute. You will be redirected to the HOME page after session timeout. Please click the button to continue session from the same page.