Home Chemistry Organic Building Blocks Alkenyls 5H-Dibenzo[B,F]Azepine
Aromatic Substitution Reactions: Dibenzazepine has two aromatic rings, which can undergo electrophilic aromatic substitution reactions. For example, it can react with electrophiles like nitronium ion (NO2+4) or sodium borohydride (NaBH4).
Oxidation Reactions: The alcohol group in 5H-dibenzo[b,f]azepine can be oxidized to a ketone or carboxylic acid using oxidizing agents like chromic acid (H2CrO4) or potassium permanganate (KMnO4).
Ring Cleavage Reactions: Depending on the reaction conditions, it might be possible to cleave one of the rings in 5H-dibenzo[b,f]azepine, generating smaller, more functionalized fragments.
Halogenation Reactions: The benzene rings can undergo halogenation reactions using halogenating agents like bromine or chlorine.
Amination Reactions: The nitrogen in the azepine ring can undergo reactions with electrophiles or nucleophiles, leading to the introduction of substituents.
Metalation Reactions: The nitrogen atoms can serve as sites for metalation reactions, where a metal atom or ion replaces a hydrogen atom on the nitrogen.
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10-Bromo-5H-dibenzo[b,f]azepine-5-carboxamide
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