Home Chemistry Organic Building Blocks Ethers 2-(Benzyloxy)Naphthalene
Nucleophilic Substitution: The benzyloxy group can undergo nucleophilic substitution reactions, such as SN1 or SN2, depending on the conditions and the nucleophile used. For example, if you treat 2-(benzyloxy)naphthalene with a strong nucleophile like sodium hydroxide (NaOH), it can lead to the displacement of the benzyloxy group by the hydroxide ion.
Aromatic Electrophilic Substitution: The naphthalene ring in the compound can undergo electrophilic aromatic substitution reactions. This includes reactions like Friedel-Crafts acylation or alkylation, where the naphthalene ring can be functionalized with various groups.
Reduction: The benzyloxy group can be reduced to the corresponding benzyl alcohol or completely to the benzyl group using reducing agents like sodium borohydride (NaBH4) or lithium aluminum hydride (LiAlH4).
Oxidation: The compound can undergo oxidation reactions. For example, the benzyloxy group can be oxidized to the corresponding benzoic acid under appropriate conditions.
Grignard Reaction: The compound can react with a Grignard reagent, leading to the formation of new carbon-carbon bonds. This can be useful for introducing various functional groups.
Hydrogenation: The naphthalene ring can be selectively hydrogenated under suitable conditions to reduce one or more of its double bonds.
Halogenation: The naphthalene ring can undergo halogenation reactions with halogens or reagents like N-bromosuccinimide (NBS), leading to the addition of halogen atoms to the ring.
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2-(Benzyloxy)-1-bromo-6-methoxynaphthalene
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(2-(Benzyloxy)naphthalen-1-yl)boronic acid
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