Home Chemistry Organic Building Blocks Ketones Cyclobutanone
Nucleophilic Addition: Cyclobutanone can undergo nucleophilic addition reactions with nucleophiles such as Grignard reagents, organolithium compounds, and primary amines, leading to the formation of various products.
Ring Expansion: Under certain conditions, cyclobutanone can undergo ring expansion reactions to form larger cyclic or acyclic compounds.
Enolate Chemistry: Cyclobutanone can be treated with strong bases to form an enolate ion, which can then undergo various reactions such as alkylation, acylation, and nucleophilic additions.
Photochemical Reactions: Cyclobutanone can undergo photochemical reactions, such as photodissociation or photorearrangements, when exposed to UV light.
Wolff-Kishner Reduction: Cyclobutanone can be converted to cyclobutylmethanamine through a Wolff-Kishner reduction reaction using hydrazine and a strong base.
Beckmann Rearrangement: Under certain conditions, cyclobutanone can undergo the Beckmann rearrangement to form a four-membered cyclic amide.
Haloform Reaction: Cyclobutanone can undergo a haloform reaction with halogens (e.g., chlorine or bromine) in the presence of a strong base, leading to the formation of haloform compounds.
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3-(2-(6-(tert-Butyl)-1H-benzo[d]imidazol-2-yl)ethyl)cyclobutanone hydrochloride
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1-Methyl-2-oxocyclobutane-1-carbonitrile
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Diisopropyl 3-oxocyclobutane-1,1-dicarboxylate
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tert-butyl N-[(3-oxocyclobutyl)methyl]carbamate
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3-((tert-Butyldimethylsilyl)oxy)cyclobutanone
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Methyl 3-oxo-1-methyl-cyclobutanecarboxylate
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