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The Perkin reaction by rctn with an ethanoic anhydride and an ethanoate salt.

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First step: Add CH2(CO2Et)2 along with Na+-OEt and ethanol to benzaldehyde. (carbonyl condensation)

Second step: Add H3O+.

The Perkin reaction is an organic reaction developed by William Henry Perkin that can be used to make cinnamic acids i.e. α-β-unsaturated aromatic acid by the aldol condensation of aromatic aldehydes and acid anhydrides in the presence of an alkali salt of the acid several reviews have been written. The reaction of phenylacetic acid and benzaldehyde with triethylamine and acetic anhydride to alpha-phenylcinnamic acid is an example of this reaction type.

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12y ago

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To convert benzaldehyde to cinnamic acid, you can use the Perkin reaction. In this reaction, benzaldehyde is treated with acetic anhydride in the presence of a basic catalyst like sodium acetate to form cinnamic acid. The reaction proceeds through an aldol condensation followed by a dehydration step to give the final product.

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10mo ago
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Q: How will you convert benzaldehyde to cinnamic acid?
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