Friedel-Crafts Acylation

时间: Invalid Date
作者: 百灵威
分享:
Friedel-Crafts Acylation-百灵威

Adding a keto group to an aromatic or aliphatic substrate using an acyl halide or anhydride in the presence of a Lewis acid catalyst is called the Friedel-Crafts acylation. The reactive electrophile in this aromatic substitution is either an acylium ion or an acyl chloride-Lewis acid complex. [1] Benzene and slightly deactivated derivatives tend to go through the acylium ion. [2] The aryl ketone can be converted to an alkyl chain via catalytic hydrogenation or the Clemmensen or Wolff-Kishner reduction.

Lab Tips:
  • Electron donating groups on the ring are often required to obtain the desired ketone in good yields. Aromatic rings with strong electron-withdrawing groups do not undergo acylation. [3]
  • Quinolines and pyridines also do not undergo acylation, but the Minisci reaction can be used to introduce acyl groups directly onto heteroaromatic rings. [3]
  • Order of reactivity: acyl iodides > acyl bromides > acyl chlorides > acyl fluorides. [3]
  • Very reactive acylating agents such as acyloxy triflates or very electron-rich substrates require little or no catalyst. [4]
  • More than one equivalent of the Lewis acid is needed since the acylating agent itself coordinates with one equivalent of the Lewis acid. [3]
  • Acylations never occur more than once as the acylated product deactivates the ring to further attack. [3]
  • Lewis basic functional groups such as amines should be protected as acylations will preferentially take place on these functional groups instead of the aromatic ring. [3]
1. Jensen, F. R., Goldman, G. (1964). Friedel-Crafts and related reactions, Vol. III, Chapter XXXVI (Olah, G. ed.). New York: Interscience Publishers Inc.
2. Sato, Y., Yato, M., Ohwada, T., Saito, S., Shudo, K. Involvement of dicationic species as the reactive intermediates in Gattermann, Houben-Hoesch, and Friedel-Crafts reactions of nonactivated benzenes. J. Am Chem. Soc. 1995, 117, 3037-3043.
3. Kürti, L., Czakó, B. (2005). Strategic Applications of Named Reactions in Organic Synthesis; Background and Detailed Mechanisms. Burlington, MA: Elsevier Academic Press.
4. Pearson, D. E., Buehler, C. A. Friedel-Crafts acylations with little or no catalyst. Synthesis 1972, 533-542.
  • Reagents: Lewis Acid (AlX3, FeCl3, Lanthanide Triflates, etc.) or Protic Acid (H2SO4, H3PO4)
  • Reactant: Aromatic, Acyl Halide or Anhydride
  • Product: Aryl Ketone
  • Type of Reaction: Electrophilic Substitution
Mechanism
Original Paper
Top Citations
Related Reactions
Related Compounds
  • Aromatic
  • Acyl halide
  • Anhydride
    advertisement