Home Chemistry Organic Building Blocks Aryls 2-Phenoxytetrahydro-2H-Pyran-4-Yl Acetate
Ester Hydrolysis: The acetate functional group may undergo hydrolysis in the presence of an acid or a base, resulting in the formation of the corresponding carboxylic acid and alcohols.
Nucleophilic Substitution: The acetyl group (acetate) can undergo nucleophilic substitution reactions with nucleophiles (e.g., amines or alcohols) in the presence of a catalyst, resulting in the formation of a new ester or amides.
Oxidation: The benzyl carbon in the phenoxy group may be susceptible to oxidation under certain conditions, leading to the formation of a carboxylic acids.
Ring Opening: The tetrahydro-2H-pyran ring may undergo ring-opening reactions under specific conditions, depending on the reagents and reaction conditions. This could result in the formation of open-chain compounds.
Esterification: The hydroxyl group in the tetrahydro-2H-pyran ring could potentially participate in esterification reactions with carboxylic acids.
Reduction: The carbonyl group in the acetate functionality may undergo reduction reactions, leading to the formation of an alcohol
Ether Formation: The hydroxyl group in the tetrahydro-2H-pyran ring may participate in reactions to form ethers, especially with alkyl halides or other suitable electrophiles.
Acetylation: The hydroxyl group could be acetylated under specific conditions, leading to the formation of an acetyl ether.
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4-Methoxyphenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside
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4-Methoxyphenyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside
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4-Methylphenyl tetra-O-acetyl-β-D-galactopyranoside
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