Home Chemistry Heterocyclic Building Blocks Tetrahydropyrans 4-Phenoxytetrahydro-2H-Pyran
Acid-Catalyzed Cleavage: The tetrahydro-2H-pyran ring may be susceptible to acid-catalyzed cleavage, leading to the formation of various products depending on the reaction conditions.
Oxidation: The phenoxy group can be oxidized under certain conditions, potentially leading to the formation of a phenol derivative.
Grignard Reactions: 4-Phenoxytetrahydro-2H-pyran may undergo reactions with Grignard reagents, leading to the addition of an alkyl or aryl group to the pyran ring.
Reduction: The compound can be reduced using reducing agents like lithium aluminum hydride (LiAlH4) to form a compound with saturated bonds.
Esterification: The phenoxy group can undergo esterification reactions with carboxylic acids and acid chlorides, forming phenoxyalkyl esters.
Halogenation: The compound may undergo halogenation reactions with halogenating agents like bromine or chlorine, leading to the addition of halogen atoms to the molecule.
Acylation: The compound can be acylated using acylating agents to introduce acyl groups onto the molecule.
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(3-Fluoro-4-((tetrahydro-2H-pyran-4-yl)oxy)phenyl)methanamine
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5-Bromo-2-((tetrahydro-2H-pyran-4-yl)oxy)benzonitrile
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(3-Methoxy-4-((tetrahydro-2H-pyran-4-yl)oxy)phenyl)methanamine
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