Home Chemistry Heterocyclic Building Blocks Morpholines Morpholino(Phenyl)Methanone
Nucleophilic Addition Reactions: The oxygen in the carbonyl group (C=O) can react with nucleophiles. For instance, in the presence of a strong nucleophile, such as a primary amine, the oxygen atom could be attacked, leading to the formation of an imine or aminal.
Reduction Reactions: The carbonyl group (C=O) can be reduced to an alcohol (C-OH) using reducing agents like lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4).
Acid-Catalyzed Reactions: The carbonyl oxygen can be protonated, which can facilitate nucleophilic addition reactions. For example, in the presence of an acid, an alcohol or water molecule may add across the carbonyl group.
Base-Catalyzed Reactions: The compound may undergo reactions where the nitrogen or oxygen atoms act as nucleophiles. For example, in the presence of a strong base, the nitrogen could potentially attack electrophiles.
Photochemical Reactions: Depending on the wavelength of light and the presence of sensitizers or photoredox catalysts, photochemical reactions may occur.
Oxidation Reactions: The compound may undergo oxidation, potentially converting the carbonyl group to a carboxylic acid or other oxidized functional groups.
Grignard Reactions: Depending on the nature of the morpholino group, it might react with a Grignard reagent, forming a new C-C bond.
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3-(Morpholine-4-carbonyl)phenylboronic acid
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(3-Fluoro-4-(morpholine-4-carbonyl)phenyl)boronic acid
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(3-(Morpholine-4-carbonyl)-5-nitrophenyl)boronic acid
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(4-Chloro-3-(morpholine-4-carbonyl)phenyl)boronic acid
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(4-(Morpholine-4-carbonyl)phenyl)boronic acid
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