Home Chemistry Organic Building Blocks Ethers 1,3-Bis(Benzyloxy)Benzene
Oxidation: The benzyl groups can be oxidized to form benzaldehyde or further to benzoic acid derivatives.
Reduction: The benzyl groups can be reduced to form tetrahydro-1,3-bis(benzyloxy)benzene.
Ether Cleavage: The ether linkages can be cleaved under acidic or basic conditions to produce the corresponding benzylic alcohols and phenols.
Substitution Reactions: The benzyl groups can undergo nucleophilic substitution reactions, for instance, with strong nucleophiles like Grignard reagents.
Friedel-Crafts Reactions: The aromatic ring can undergo Friedel-Crafts reactions with suitable electrophiles in the presence of a Lewis acid catalyst.
Esterification: The benzyloxy groups can be converted into esters using appropriate reagents, such as acid chlorides and a base.
Cleavage of Carbon-Oxygen Bonds: The C-O bonds in the benzyloxy groups can be cleaved using reagents like boron tribromide (BBr3) or thionyl chloride (SOCl2).
Polymerization: The benzyloxy groups can be used as reactive sites for polymerization reactions, especially when there are multiple benzyloxy groups on the same molecule.
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