Friedel-Crafts Acylation

Definition

Friedel-Crafts acylation is a type of electrophilic aromatic substitution reaction in organic chemistry where an acyl group is introduced onto an aromatic ring in the presence of a Lewis acid catalyst. This reaction is used to synthesize aromatic ketones and is an important tool in the construction of more complex organic molecules.

5 Must Know Facts For Your Next Test

1. Friedel-Crafts acylation involves the reaction of an acyl halide (e.g. acetyl chloride) with an aromatic compound in the presence of a Lewis acid catalyst (e.g. aluminum chloride).
2. The Lewis acid catalyst coordinates to the carbonyl oxygen of the acyl halide, making the carbonyl carbon more electrophilic and susceptible to attack by the aromatic ring.
3. Friedel-Crafts acylation typically occurs at the most nucleophilic position on the aromatic ring, usually the ortho or para position relative to any existing substituents.
4. The reaction is regioselective, meaning it favors the formation of one regioisomeric product over others, depending on the substitution pattern of the aromatic starting material.
5. Friedel-Crafts acylation is a useful method for the synthesis of polysubstituted benzenes, as the acyl group can be further functionalized through subsequent reactions.

Review Questions

• Explain the role of the Lewis acid catalyst in Friedel-Crafts acylation and how it facilitates the reaction.
  • The Lewis acid catalyst, such as aluminum chloride (AlCl3), plays a crucial role in Friedel-Crafts acylation. It coordinates to the carbonyl oxygen of the acyl halide reactant, making the carbonyl carbon more electrophilic and susceptible to attack by the aromatic ring. This activation of the acyl halide by the Lewis acid is a key step that enables the electrophilic aromatic substitution to occur, leading to the formation of the desired aromatic ketone product.
• Describe the regiochemistry of Friedel-Crafts acylation and how it is influenced by the substitution pattern of the aromatic starting material.
  • Friedel-Crafts acylation is a regioselective reaction, meaning that it favors the formation of one regioisomeric product over others. The substitution pattern of the aromatic starting material plays a significant role in determining the preferred site of acylation. Generally, the acyl group will be introduced at the most nucleophilic position on the aromatic ring, which is typically the ortho or para position relative to any existing substituents. The presence and nature of these substituents can influence the reactivity and directing effects, leading to the selective formation of the desired regioisomer.
• Explain how Friedel-Crafts acylation can be utilized in the synthesis of polysubstituted benzenes, and discuss the importance of this transformation in organic chemistry.
  • Friedel-Crafts acylation is a valuable tool for the synthesis of polysubstituted benzenes, as the acyl group introduced onto the aromatic ring can be further functionalized through subsequent reactions. For example, the aromatic ketone product of the Friedel-Crafts acylation can undergo additional transformations, such as reduction, halogenation, or alkylation, to generate more complex aromatic compounds. This versatility makes Friedel-Crafts acylation an important reaction in organic synthesis, as it allows for the construction of a wide range of substituted benzene derivatives, which are prevalent in many natural products, pharmaceuticals, and other important organic molecules.

Related terms

Electrophilic Aromatic Substitution: A class of reactions where an electrophile replaces a hydrogen atom on an aromatic ring, resulting in the formation of a new carbon-carbon bond.

Lewis Acid: A species that can accept a pair of electrons, commonly used as a catalyst in Friedel-Crafts reactions to activate the acyl halide reactant.

Aromatic Ketone: A carbonyl compound where the carbonyl group is attached directly to an aromatic ring, formed as the product of Friedel-Crafts acylation.