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2-Bromotetrafluoroethyl aryl ethers

Later on, a more efficient and mild way to prepare this compound in a two-step process (Scheme 14.2) was revealed by Babb et al. in 1993 [4], Starting from phenolic precursors, the first step is fluoroalkylation with 1,2-dibromotetrafluoroethane (BrCF2CF2Br) to give 2-bromotetrafluoroethyl aryl ethers. In this reaction, BrCF2CF2Br (widely used as nontoxic fire extinguishing agent) served as a fluoroalkylation agent and as a trifluorovinyl precursor. [Pg.345]

See other pages where 2-Bromotetrafluoroethyl aryl ethers is mentioned: [Pg.45]    [Pg.31]    [Pg.341]    [Pg.31]    [Pg.45]    [Pg.31]    [Pg.341]    [Pg.31]   
See also in sourсe #XX -- [ Pg.3 , Pg.41 ]

See also in sourсe #XX -- [ Pg.3 , Pg.41 ]

See also in sourсe #XX -- [ Pg.3 , Pg.41 ]



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Aryl ethers

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