Instead it is prepared by the Sandmeyer reaction from 3,5-dichloro aniline.

An example of this reaction type is the Sandmeyer reaction.

The second main route is the Sandmeyer reaction.

Sandmeyer reactions with copper salts used in catalytic amounts are also known.

Iodobenzene is commercially available, but it may be prepared in the laboratory from aniline via the Sandmeyer reaction.

This is the Sandmeyer reaction.

Amyl nitrites are also useful as reagents in a modification of the Sandmeyer reaction.

Aromatic iodides may be prepared via a diazonium salt in the Sandmeyer reaction.

The majority of variations of the Sandmeyer reactions consist of using various copper salts.

It follows Sandmeyer reaction.

This reaction is simpler than the Sandmeyer reaction, but is only applicable for compounds that are stable enough to survive the high temperature.

The reaction is similar to the Sandmeyer reaction, which converts diazonium salts to other aryl halides.

In the Sandmeyer reaction and the Gattermann reaction diazonium salts react with halides.

The Sandmeyer reaction is a chemical reaction used to synthesize aryl halides from aryl diazonium salts.

In the Sandmeyer reaction, CuBr is employed to convert diazonium salts into the corresponding aryl bromides:

These transformations are associated with many named reactions including the Schiemann reaction, Sandmeyer reaction, and Gomberg-Bachmann reaction.

In this step, the Sandmeyer reaction converts the primary amino group (NH) to a diazonium leaving group (N), which is subsequently replaced by iodine.

Through these intermediates, aniline can be conveniently converted to -OH, -CN, or a halide via Sandmeyer reactions.

Potassium iodine finds its most important applications in organic synthesis mainly in the preparation of aryl iodides in the Sandmeyer reaction, starting from aryl amines.

The process is a formal nucleophilic aromatic substitution reaction, is the basis of the Sandmeyer Reaction, the Gomberg-Bachmann reaction and the Schiemann reaction.

Such salts are widely used in organic synthesis, e.g., for the Sandmeyer reaction and in the preparation azo dyes, brightly colored compounds that are the basis of a qualitative test for anilines.

The improved Sandmeyer reaction using metallic copper as catalyst, and the discovery of the reaction of hydrocyanic acid with an aromatic compound now called the Gatterman reaction were achieved during his time in Heidelberg.

It may include the reaction where a diazonium salt is converted to an aryl halide by using copper powder and hydrochloric acid as opposed to using cuprous salt of the halide as in the Sandmeyer reaction.