Home Chemistry Organic Building Blocks Carboxylic Acids 2-Methyl-2-Phenylpropanoic Acid
These compounds have the same murcko framework: benzene,and at least 1 kind of functional groups( —C(CH3)2COOH).
Esterification: α-Toluic acid can undergo esterification reactions with 【alcohols|https://www.ambeed.com/alcohols.html】 in the presence of an acid catalyst to form 【esters|https://www.ambeed.com/esters.html】. For example, with methanol (CH3OH) and sulfuric acid (H2SO4) as a catalyst, you would get methyl α-toluate.
Decarboxylation: Under certain conditions, 【carboxylic acids|https://www.ambeed.com/carboxylic-acids.html】 can undergo decarboxylation reactions, losing a carbon dioxide molecule and forming a substituted benzene ring. The specific conditions required for this reaction can vary.
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2-(3-Methoxyphenyl)-2-methylpropanoic acid
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2-(4-Ethylphenyl)-2-methylpropanoic acid
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2-(4-Boronophenyl)-2-methylpropanoic acid
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2-(2-Methoxyphenyl)-2-methylpropanoic acid
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2-(4-Chlorophenyl)-2-methylpropanoic acid
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2-(4-Ethyl-3-iodophenyl)-2-methylpropanoic acid
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2-(2,6-Difluorophenyl)-2-methylpropanoic acid
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2-(2-Fluorophenyl)-2-methylpropanoic acid
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2-(3,4-Dichlorophenyl)-2-methylpropanoic acid
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2-(3,5-Bis(trifluoromethyl)phenyl)-2-methylpropanoic acid
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(E)-2-(4-((2-Cyanovinyl)sulfonyl)phenyl)-2-methylpropanoic acid
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2-(4-Hydroxyphenyl)-2-methylpropanoic acid
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2-(4-(2-Hydroxyethyl)phenyl)-2-methylpropanoic acid
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