Issue 94, 2024

Accessing structurally diverse aryl difluoromethyl ethers with bromo(difluoro)acetic acid

Abstract

We report a new streamlined approach for the difluoromethylation of ubiquitous phenols using inexpensive bromo(difluoro)acetic acid, yielding a wide array of structurally diverse OCF2H-based building blocks in a single step. This method displays broad functional group compatibility and is amenable for effective late-stage diversification and lignin-derived monomers.

Graphical abstract: Accessing structurally diverse aryl difluoromethyl ethers with bromo(difluoro)acetic acid

Supplementary files

Article information

Article type
Communication
Submitted
16 Sep 2024
Accepted
17 Oct 2024
First published
18 Oct 2024

Chem. Commun., 2024,60, 13935-13938

Accessing structurally diverse aryl difluoromethyl ethers with bromo(difluoro)acetic acid

S. Kumawat and K. Natte, Chem. Commun., 2024, 60, 13935 DOI: 10.1039/D4CC04782F

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