Sandmeyer Reactions

Sandmeyer reactions are an incredibly powerful set of transformations that can convert a C-N bond in an aromatic molecule to a variety of carbon-heteroatom, carbon-carbon, and carbon-H bonds.

To make aryl diazonium salts:

  1. Start from a nitrobenzene and reduce the nitro group to an aniline with hydrogen and palladium on carbon or Sn/HCl or Fe/ammonium chloride.

  2. Diazotize the aniline with sodium nitrite and acid (forms nitrous acid in situ)

You can take an aryl diazonium salt and convert it to many different things!

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Friedel-Crafts Alkylation and Acylation

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Functional Groups that you should memorize for organic chemistry