Benzyl 4-bromophenyl ether

C13H11BrO benzyl 4-bromophenyl ether 6793-92-6 25.00 1.4024 2 25811 C13H1202 1 -methoxy-2-phenoxybenzene 1695-04-1 21.25 1.1359 2... 

Benzyl ic ethers Tris (p-bromophenyl)amine Fast deprotonation of radical cation in the presence of a soluble base [117]... 

The siloxy compound and benzyl chloride treated with tetrabutylammonium fluoride 3 HjO in THF and left at ambient temp, (for 16h) gave benzy l 4-bromophenyl ether... 

BRN 1912585, see Hexachlorobenzene BRN 1912384, see 2,4-Dinitrotoluene BRN 1913355, seep,p -DDE BRN 1914064, see Di-fl-butyl phthalate BRN 1914072, see p,p -DDD BRN 1915474, see Chlordane BRN 1915994, see Di-fl-octyl phthalate BRN 2049930, see Naled BRN 2051258, see Pindone BRN 2052046, see 2,6-Dinitrotoluene BRN 2054389, see 4,6-Dinitro-o-cresol BRN 2055620, see 2,4,5-T BRN 2057367, see Methoxychlor BRN 2059093, see Parathion BRN 2062204, see Benzyl butyl phthalate BRN 2215168, see Diuron BRN 2542580, see EPN BRN 2807677, see 2-Acetylaminofluorene BRN 3195880, see a-BHC BRN 3196099, see Camphor BRN 3910347, see cis-Chlordane, frans-Chlordane Brocide, see 1,2-Dichloroethane Brodan, see Chlorpyrifos Bromchlophos, see Naled Bromex, see Naled Bromic ether, see Ethyl bromide Bromobenzol, see bromobenzene 4-Bromobiphenyl ether, see 4-Bromophenyl phenyl ether 4-Bromodiphenyl ether, see 4-Bromophenyl phenyl ether p-Bromodiphenyl ether, see 4-Bromophenyl phenyl ether Bromoethane, see Ethyl bromide Bromofluoroform, see Bromotrifluoromethane Bromofume, see Ethylene dibromide Brom-o-gaz, see Methyl bromide Bromomethane, see Methyl bromide Bromomethyl chloride, see Bromochloromethane... 

Last year in this Report (3,156) the oxidative removal of p-methoxybenzyl ethers, by homogeneous electron transfer from the stable cation radical of tris-(4-bromophenyl)amine, was featured. This procedure did not affect benzyl ethers, but a recent extension of these studies to cation radicals (61), of higher oxidation potential, has allowed development of methods to cleave benzyl protecting groups from alcohols [equation (10)]. The radicals may, as in the earlier report, be used either stoicheiometrically, or catalytically and regenerated electrochemically in situ. The potential selectivity between different benzyl type protecting groups now available by this method has been illustrated in a further publication. ... 

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