Home Chemistry Heterocyclic Building Blocks Azetidines 1-Benzhydrylazetidine
Ring Opening Reactions: Azetidine rings can undergo ring-opening reactions under certain conditions. This can involve breaking one of the carbon-nitrogen bonds in the azetidine ring to open the ring. The exact conditions and mechanisms will depend on the specific reaction conditions.
Nucleophilic Substitution: If there are suitable leaving groups or electrophilic sites in the molecule, 1-benzhydrylazetidine can undergo nucleophilic substitution reactions. Nucleophiles can attack electrophilic centers in the molecule, leading to the displacement of a leaving group.
Oxidation Reactions: Depending on the functional groups present in the molecule, 1-benzhydrylazetidine can undergo oxidation reactions. Oxidation can lead to the formation of new functional groups or the cleavage of existing bonds.
Reduction Reactions: Similarly, 1-benzhydrylazetidine can undergo reduction reactions if there are suitable functional groups that can be reduced. Common reducing agents like lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) can be used.
Grignard Reactions: 1-Benzhydrylazetidine can react with Grignard reagents to form new carbon-carbon bonds. This can be a useful method for introducing alkyl or aryl groups to the molecule.
Acid-Catalyzed Reactions: Depending on the reaction conditions, acid-catalyzed reactions such as acylation or alkylation may be possible with 1-benzhydrylazetidine.
Base-Catalyzed Reactions: Base-catalyzed reactions like deprotonation or elimination reactions may also occur if appropriate conditions are provided.
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1-(Diphenylmethyl)azetidine-3-carboxylic Acid
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Methyl 1-benzhydrylazetidine-3-carboxylate
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tert-Butyl ((1-benzhydrylazetidin-3-yl)methyl)carbamate
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1-Benzhydryl-3-(methoxymethyl)azetidine
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1-Benzhydryl-3-methylazetidin-3-yl methanesulfonate
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1-Benzhydrylazetidin-3-yl methanesulfonate
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1-(Diphenylmethyl)azetidine-3-carbonitrile
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