Home Chemistry Heterocyclic Building Blocks Pyrans Dihydro-2H-Pyran-2,6(3H)-Dione
Aromatic Substitution: The phenyl groups in 1,3-diphenylpropane can undergo electrophilic aromatic substitution reactions, such as nitration, halogenation, sulfonation, or Friedel-Crafts acylation/alkylation, to introduce different functional groups onto the phenyl rings.
Hydrogenation: 1,3-diphenylpropane can be hydrogenated using a catalyst like palladium or platinum to convert the carbon-carbon double bonds into single bonds, leading to 1,3-diphenylpropane.
Oxidation: Oxidation reactions, such as using strong oxidizing agents like chromic acid (H2CrO4) or potassium permanganate (KMnO4), can convert the alkyl chains into corresponding carboxylic acids or other functional groups.
Halogenation: The alkyl chain can undergo halogenation reactions, such as bromination or chlorination, which replace hydrogen atoms with halogens.
Reduction: Reduction with strong reducing agents like lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) can convert carbonyl groups (if present) into alcohol functional groups.
Grignard Reaction: The compound can be used as a substrate for Grignard reactions, where a Grignard reagent (RMgX) adds to the carbonyl group to form alcohol or other derivatives.
Friedel-Crafts Acylation: The aromatic rings can undergo acylation reactions with acyl halides or anhydrides in the presence of a Lewis acid catalyst, such as aluminum chloride (AlCl3).
Alkylation: In a Friedel-Crafts alkylation reaction, the aromatic rings can be alkylated using alkyl halides and a Lewis acid catalyst.
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3,3-Dimethyldihydro-2H-pyran-2,6(3H)-dione
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3-(tert-Butyldimethylsilyloxy)glutaric anhydride
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