Which base is use in Knovengel reaction ?
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A Knoevenagel condensation is demonstrated in the reaction of 2-methoxybenzaldehyde 1 with the thiobarbituric acid 2 in ethanol using piperidine as a base. The resulting enone 3 is a charge transfer complex
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Amine base is used as a catalyst in the Knoevenagel reaction.
- The Knoevenagel condensation is an organic reaction that converts a carbonyl functional group (aldehyde or ketone) and activated methylene (esters) into a substituted olefin (alkene).
- An amine base is used as a catalyst. It is not consumed during the reaction and it speeds up the reaction rate.
- The amine catalyst reacts with the aldehyde or ketone to form an iminium ion intermediate.
- The intermediate then gets attacked by the enolate and gets deprotonated by the base.
- Rearrangement happens that gives the final product and the base is released.
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