Azo coupling

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An azo coupling is an organic reaction between a diazonium compound and another aromatic compound that produces an azo compound. In this electrophilic aromatic substitution reaction, the aryldiazonium cation is the electrophile and the activated arene is a nucleophile.[1] In most cases, including the examples below, the diazonium compound is also aromatic.

Diazotization[]

The process of conversion of primary aromatic amines into its diazonium salt is called diazotization. Diazonium salts are important synthetic intermediates that can undergo coupling reactions to form azo dyes and electrophilic substitution reactions to introduce functional groups.

Uses of the reaction[]

Aromatic azo compounds tend to be brightly colored due to the extended . Many are used as dyes (see azo dye).[2] Important azo dyes include methyl red and pigment red 170. Azo printing exploits this reaction as well.[3]

Azo coupling is also used to produce prontosil and other sulfa drugs.

Examples of azo C-coupling reactions[]

Many procedures have been described.[4][5] Phenol reacts with benzenediazonium chloride to give a Solvent Yellow 7, a yellow-orange azo compound. The reaction is base-catalysed.[2]

Azo-coupling-A-mechanism-2D-skeletal.png

The related dye called aniline yellow is produced from the reaction of aniline and the diazonium salt.[2] Naphthols are popular acceptors. One example is the synthesis of the dye "organol brown" from aniline and 1-naphthol:

Organol brown synthesis

Similarly β-naphthol couples with phenyldiazonium electrophile to produce an intense orange-red dye.

Examples of azo N-coupling reactions[]

Azo N-coupling

In alkaline media, diazonium salt can react with most primary and secondary amines that exist as a free base and produce triazene.[6] This chemical reaction is called azo N-coupling[7] or the synthesis of azoamines.[8]

Synthesis of C.I. Pigment Yellow 12, a diarylide pigment.

References[]

  1. ^ Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, ISBN 978-0-471-72091-1
  2. ^ a b c Klaus Hunger; Peter Mischke; Wolfgang Rieper; Roderich Raue; Klaus Kunde; Aloys Engel (2005). Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a03_245.
  3. ^ Pai, Damodar M.; Melnyk, Andrew R.; Weiss, David S.; Hann, Richard; Crooks, Walter; Pennington, Keith S.; Lee, Francis C.; Jaeger, C. Wayne; Titterington. "Imaging Technology, 2. Copying and Nonimpact Printing Processes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. pp. 1–53. doi:10.1002/14356007.o13_o08.pub2.
  4. ^ J. L. Hartwell and Louis F. Fieser. "Coupling of o-tolidine and Chicago acid". Organic Syntheses.; Collective Volume, 2, p. 145
  5. ^ H. T. Clarke and W. R. Kirner. "Methyl red". Organic Syntheses.; Collective Volume, 1, p. 374
  6. ^ Khazaei; et al. (2012). "azo amine coupling giving triazenes, and triazene's decomposition giving diazonium salt". Synlett. 23 (13): 1893–1896. doi:10.1055/s-0032-1316557.
  7. ^ Wiley Subscription Services (2013). "Synthesis, characterization, and application of a triazene-base polymer". Journal of Applied Polymer Science. 129 (6): 3439–3446. doi:10.1002/app.39069.
  8. ^ Serge Ratton, Bernard Botannet (1981). "Preparation of aromatic azoamines by diazotization/coupling/rearrangement of aromatic amines". US Patent 4275003A.
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