Home Chemistry Organic Building Blocks Ethers 2-(Phenoxymethyl)Oxirane
Ring Opening Reactions: The most common reaction for Epoxides like 2-(phenoxymethyl)oxirane is ring opening. This can occur through various mechanisms, including nucleophilic attack. For example, nucleophiles like water, alcohols, amines, and others can open the epoxide ring to form diols, alcohols, or amines, depending on the nature of the nucleophile. The reaction might be acid-catalyzed or base-catalyzed.
Epoxide Ring Cleavage: Under acidic conditions, the epoxide ring can undergo cleavage to form a carbocation intermediate. This intermediate can then react further with nucleophiles.
Halogenation: Epoxides can undergo halogenation reactions in the presence of halogenating agents like HX or N-halosuccinimide to yield halohydrin products.
Polymerization: Epoxides like 2-(phenoxymethyl)oxirane can undergo polymerization reactions when treated with suitable initiators or catalysts. This is the basis for the formation of epoxy resins, which are widely used in various industries.
Substitution Reactions: The phenyl group in 2-(phenoxymethyl)oxirane can undergo substitution reactions. For example, it can react with nucleophiles in an aromatic substitution reaction.
Epoxide Rearrangements: Under certain conditions, Epoxides can undergo rearrangement reactions, leading to the formation of different products. For example, the rearrangement of Epoxides can yield aldehydes or ketones.
Epoxy Ring Cleavage: In the presence of suitable reagents and conditions, the epoxy ring can be cleaved to form compounds with open-chain structures.
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3-[4-(2-Methoxyethyl)phenoxy]-1,2-epoxypropane
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2-{4-[(Oxiran-2-yl)methoxy]phenyl}acetic acid
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2-((4-((2-Isopropoxyethoxy)methyl)phenoxy)methyl)oxirane
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