Home Chemistry Organic building blocks Ethers Phenethoxybenzene
Williamson Ether Synthesis: Phenetole can be synthesized using the Williamson ether synthesis by reacting a phenoxide ion (obtained from phenol) with ethyl halides (e.g., ethyl bromide or ethyl chloride) in the presence of a strong base like sodium hydroxide (NaOH).
Acid-Catalyzed Cleavage: Phenetole can be cleaved by strong acids, such as concentrated hydrochloric acid or sulfuric acid. This reaction can lead to the formation of phenol and ethyl alcohol as products.
Electrophilic Aromatic Substitution: The phenyl group in phenetole can undergo electrophilic aromatic substitution reactions, such as nitration, sulfonation, halogenation, or Friedel-Crafts acylation or alkylation.
Oxidation: Phenetole can be oxidized to form different compounds, depending on the reagents and conditions used. Common oxidizing agents include hydrogen peroxide (H2O2) or potassium permanganate (KMnO4).
Photolysis: Exposure to ultraviolet (UV) light can lead to the cleavage of the ether bond in phenetole, resulting in the formation of phenol and ethyl radicals.
Reductive Cleavage: Under certain conditions, phenetole can undergo reductive cleavage reactions using reducing agents like lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4).
Hydrolysis: Phenetole can be hydrolyzed in the presence of strong acids or bases to yield phenol and ethyl alcohol as products.
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1-(3,4-Dimethoxyphenyl)-2-(2-methoxyphenoxy)propane-1,3-diol
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