Home Chemistry Organic Building Blocks Ketones Ethyl 3-Oxo-3-Phenylpropanoate
These compounds have the same murcko framework: benzene,and at least 1 kind of functional groups( —C(O)CH2COOC2H5).
Nucleophilic Addition: Compounds with a carbonyl group (like 【ketones|https://www.ambeed.com/ketones.html】) are susceptible to nucleophilic addition reactions. Nucleophiles can attack the electrophilic carbon of the carbonyl group, leading to the formation of a new compound. For example, you could react ethyl 3-oxo-3-phenylpropanoate with a strong nucleophile like a Grignard reagent (e.g., phenylmagnesium bromide) to form a tertiary 【alcohol|https://www.ambeed.com/alcohols.html】 after hydrolysis.
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Ethyl 3-(2,6-Difluorophenyl)-3-oxopropionate
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Ethyl 3-oxo-3-(4-(trifluoromethyl)phenyl)propanoate
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Ethyl 3-(2-hydroxyphenyl)-3-oxopropanoate
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Ethyl 3-(2,5-difluorophenyl)-3-oxopropanoate
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Ethyl 3-(3-((tert-butoxycarbonyl)amino)phenyl)-3-oxopropanoate
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Ethyl 3-(2-fluoro-4-methoxyphenyl)-3-oxopropanoate
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Ethyl 3-(3-chloro-2,4,5-trifluorophenyl)-3-oxopropanoate
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Ethyl 3-(3,5-difluorophenyl)-3-oxopropanoate
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Ethyl 3-(2,6-dichlorophenyl)-3-oxopropanoate
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