Home Chemistry Heterocyclic Building Blocks Benzofurans 4-Phenyldibenzo[B,D]Furan
Aromatic Substitution Reactions: Given the presence of an aromatic ring in the molecule, it can undergo electrophilic aromatic substitution reactions. For example, it can react with electrophiles like halogens (e.g., bromination or chlorination) or with nitration reagents (e.g., nitric acid and sulfuric acid) to introduce substituents onto the aromatic rings.
Reduction Reactions: 4-Phenyldibenzo[b,d]furan can be reduced using various reducing agents such as hydrogen gas in the presence of a metal catalyst (e.g., palladium on carbon) to yield a dihydro compound.
Oxidation Reactions: The molecule can be oxidized to introduce oxygen-containing functional groups. For instance, mild oxidizing agents like potassium permanganate can be used to oxidize the molecule.
Grignard Reactions: You can perform Grignard reactions by treating 4-phenyldibenzo[b,d]furan with a Grignard reagent (an organomagnesium compound), which can lead to the formation of new carbon-carbon bonds.
Friedel-Crafts Acylation/Alkylation: The aromatic rings in the molecule can undergo Friedel-Crafts reactions. For example, you can acylate or alkylate the aromatic rings using acyl or alkyl halides in the presence of a Lewis acid catalyst.
Hydrogenation: 4-Phenyldibenzo[b,d]furan can be hydrogenated using hydrogen gas and a suitable catalyst to convert the double bonds to single bonds, resulting in a saturated compound.
Ring-Opening Reactions: In some cases, under specific conditions and with appropriate reagents, the dibenzo[b,d]furan ring system can undergo ring-opening reactions, leading to the formation of different products.
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(6-Phenyldibenzo[b,d]furan-4-yl)boronic acid
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(3-(Dibenzo[b,d]furan-4-yl)phenyl)boronic acid
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