23.10 Conjugate Carbonyl Additions: The Michael Reaction

23.10 • Conjugate Carbonyl Additions: The Michael Reaction

We saw in Section 19.13 that certain nucleophiles, such as amines, react with α,β-unsaturated aldehydes and ketones to give a conjugate addition product, rather than a direct addition product.

Exactly the same kind of conjugate addition can occur when a nucleophilic enolate ion reacts with an α,β-unsaturated carbonyl compound—a process known as the Michael reaction after Arthur Michael at Tufts College and Harvard University.

The best Michael reactions are those that take place when a particularly stable enolate ion, such as that derived from a β-keto ester or other 1,3-dicarbonyl compound, adds to an unhindered α,β-unsaturated ketone. For example, ethyl acetoacetate reacts with 3-buten-2-one in the presence of sodium ethoxide to yield the conjugate addition product.

Michael reactions take place by addition of a nucleophilic enolate ion donor to the β carbon of an α,β-unsaturated carbonyl acceptor, according to the mechanism shown in Figure 23.7.

Figure 23.7 MECHANISM

Mechanism of the Michael reaction between a β-keto ester and an α,β-unsaturated ketone. The reaction is a conjugate addition of an enolate ion to the unsaturated carbonyl compound.

The Michael reaction occurs with a variety of α,β-unsaturated carbonyl compounds, not just conjugated ketones. Unsaturated aldehydes, esters, thioesters, nitriles, amides, and nitro compounds can all act as the electrophilic acceptor component in Michael reactions (Table 23.1). Similarly, a variety of different donors can be used, including β-diketones, β-keto esters, malonic esters, β-keto nitriles, and nitro compounds.

Table 23.1 Some Michael Acceptors and Michael Donors

Michael acceptors		Michael donors
	Propenal		β-Diketone
	3-Buten-2-one		β-Keto ester
	Ethyl propenoate		Diethyl malonate
	Propenamide		β-Keto nitrile
	Propenenitrile		Nitro compound
	Nitroethylene

Worked Example 23.5

Using the Michael Reaction

How might you obtain the following compound using a Michael reaction?

Strategy

A Michael reaction involves the conjugate addition of a stable enolate ion donor to an α,β-unsaturated carbonyl acceptor, yielding a 1,5-dicarbonyl product. Usually, the stable enolate ion is derived from a β-diketone, β-keto ester, malonic ester, or similar compound. The C–C bond formed in the conjugate addition step is the one between the α carbon of the acidic donor and the β carbon of the unsaturated acceptor.

Solution

Problem 23-16

What product would you obtain from a base-catalyzed Michael reaction of 2,4-pentanedione with each of the following α,β-unsaturated acceptors?

(a)

2-Cyclohexenone

(b)

Propenenitrile

(c)

Ethyl 2-butenoate

Problem 23-17

What product would you obtain from a base-catalyzed Michael reaction of 3-buten-2-one with each of the following nucleophilic donors?

(a)

(b)

Problem 23-18

How would you prepare the following compound using a Michael reaction (gray = H, black = C, red = O, blue = N)?