Jump to content

Acetoacetic ester synthesis

From Wikipedia, the free encyclopedia

Acetoacetic ester synthesis
Reaction type Coupling reaction
Reaction
Acetoacetic acid esters
+
R-X
+
(-O-R & H3O+)
α-substituted acetone
Conditions
Temperature
Identifiers
Organic Chemistry Portal acetoacetic-ester-synthesis
RSC ontology ID RXNO:0000107

Acetoacetic ester synthesis is a chemical reaction where ethyl acetoacetate is alkylated at the α-carbon to both carbonyl groups and then converted into a ketone, or more specifically an α-substituted acetone. This is very similar to malonic ester synthesis.

Acetoacetic ester synthesis equation
Acetoacetic ester synthesis equation

Mechanism

[edit]

A strong base deprotonates the dicarbonyl α-carbon. This carbon is preferred over the methyl carbon because the formed enolate is conjugated and thus resonance stabilized. The carbon then undergoes nucleophilic substitution. When heated with aqueous acid, the newly alkylated ester is hydrolyzed to a β-keto acid, which is decarboxylated to form a methyl ketone.[1][2] The alkylated ester can undergo a second substitution to produce the dialkylated product.

Acetoacetic ester synthesis

Double deprotonation of ethyl acetoacetate

[edit]

The classical acetoacetatic ester synthesis utilizes the 1:1 conjugate base. Ethyl acetoacetate is however diprotic:[3]

CH3C(O)CH2CO2Et + NaH → CH3C(O)CH(Na)CO2Et + H2
CH3C(O)CH(Na)CO2Et + BuLi → LiCH2C(O)CH(Na)CO2Et + BuH

The dianion (i.e., LiCH2C(O)CH(Na)CO2Et) adds electrophile to the terminal carbon as depicted in the following simplified form:[3]

LiCH2C(O)CH(Na)CO2Et + RX → RCH2C(O)CH(Na)CO2Et + LiX

See also

[edit]

References

[edit]
  1. ^ Smith, Janice Gorzynski. Organic Chemistry: Second Ed. 2008. pp 905–906
  2. ^ Acetoacetic Ester Synthesis – Alkylation of Enolates | PharmaXChange.info
  3. ^ a b Jin, Yinghua; Roberts, Frank G.; Coates, Robert M. (2007). "Stereoselective Isoprenoid Chain Extension with Acetoacetate Dianion: [(E, E, E)-Geranylgeraniol from (E, E)-Farnesol". Organic Syntheses. 84: 43. doi:10.15227/orgsyn.084.0043.