Home Chemistry Heterocyclic Building Blocks Tetrahydropyrans (S)-2-(Phenylthio)Tetrahydro-2H-Pyran
Hydrolysis: The compound may undergo hydrolysis when exposed to water or an aqueous solution. In this process, the ether linkage can be cleaved, leading to the formation of the corresponding alcohol and thiol.
Oxidation: The thiol group in the compound can be oxidized to form a disulfide bond or a sulfoxide, depending on the oxidizing agent used.
Ring Opening: The tetrahydro-2H-pyran ring can undergo ring-opening reactions under certain conditions, such as with acid catalysis or nucleophilic attack. This can lead to the formation of open-chain compounds.
Substitution Reactions: Depending on the reaction conditions and reagents used, the phenylthio group could undergo substitution reactions. For instance, it could be replaced by other groups.
Reduction: The compound may undergo reduction reactions to convert functional groups to their reduced forms. This could involve reducing the ketone group, for example.
Acylation or Alkylation: The compound can be acylated or alkylated to introduce new functional groups onto the molecule.
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