Radical-nucleophilic aromatic substitution

Radical-nucleophilic aromatic substitution or S_RN1 in organic chemistry is a type of substitution reaction in which a certain substituent on an aromatic compound is replaced by a nucleophile through an intermediary free radical species:

Additional recommended knowledge

Daily Visual Balance Check

Don't let static charges disrupt your weighing accuracy

Safe Weighing Range Ensures Accurate Results

The substituent X is a halide and nucleophiles can be sodium amide, an alkoxide or a carbon nucleophiles such as an enolate.^[1] In contrast to regular nucleophilic aromatic substitution, deactivating groups on the arene are not required.

This reaction type was discovered in 1970 by Bunnett and Kim ^[2] and the abbreviation S_RN1 stands for substitution radical-nucleophilic unimolecular as it shares properties with an aliphatic SN1 reaction. An example of this reaction type is the Sandmeyer reaction.

Reaction mechanism

In this radical substitution the aryl halide 1 accepts an electron from an radical initiator forming a radical anion 2. This intermediate collapses into an aryl radical 3 and a halide anion. The aryl radical reacts with the nucleophile 4 to a new radical anion 5 which goes on to form the substituted product by transferring its electron to new aryl halide in the chain propagation. Alternatively the phenyl radical can abstract any loose proton from 7 forming the arene 8 in a chain termination reaction.

The involvement of a radical intermediate in a new type of nucleophilic aromatic substitution was invoked when the product distribution was compared between a certain aromatic chloride and an aromatic iodide in reaction with potassium amide. The chloride reaction proceeds through a classical aryne intermediate:

The isomers 1a and 1b form the same aryne 2 which continues to react to the anilines 3a and 3b in a 1 to 1.5 ratio. Clear-cut cine-substitution would give a 1:1 ratio but additional steric and electronic factors come into play as well.

Replacing chlorine by iodine in the 1,2,4-trimethylbenzene moiety drastically changes the product distribution:

It now resembles ipso-substitution with 1a forming preferentially 3a and 1b forming 3b. Radical scavengers suppress ipso-substitution in favor of cine-substitution and the addition of potassium metal as an electron donor and radical initiator does exactly the opposite ^[3].

References

See also

• Birch reduction
• Nucleophilic aromatic substitution