Michael Addition Reaction Mechanism

TL;DR

The microreaction involves the use of a stabilized enolate ion as a micro donor to react with an alpha-beta unsaturated compound, resulting in the formation of a 1,5-dicarbonyl compound. The yield of the reaction depends on the strength of the base and the accessibility of the carbonyl carbon.

Transcript

in this video we're going to talk about the microreaction so the first thing we need is a michael donor which is typically a stabilized enolate so let's use a base to remove the alpha hydrogen in the first step and so here we have an enolate that is stabilized by two carbonyl groups and then this is going to react with an alpha beta unsaturated ald... Read More

Key Insights

• 😒 The microreaction involves the use of a stabilized enolate as a nucleophile to react with alpha-beta unsaturated compounds.
• 👊 Weak bases prefer to attack the beta carbon, while strong bases tend to attack the carbonyl carbon in the microreaction.
• ♿ The yield in the microreaction can be increased by using sterically hindered alpha-beta unsaturated ketones or reducing the accessibility of the carbonyl carbon.
• 📶 The pKa values of the conjugate acids determine the relative strength of the bases involved in the microreaction.
• 👋 Nitroethane can serve as a good micro donor due to the relative acidity of its alpha hydrogen.

Summary & Key Takeaways

• The microreaction involves a stabilized enolate ion reacting with an alpha-beta unsaturated compound.

• Weak bases tend to attack the beta carbon, resulting in conjugate addition, while strong bases attack the carbonyl carbon, leading to direct addition.

• Yield in the microreaction can be increased by using sterically hindered alpha-beta unsaturated ketones or reducing the accessibility of the carbonyl carbon.