Radical-nucleophilic aromatic substitution

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Radical-nucleophilic aromatic substitution or SRN1 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:

Radical-nucleophilic aromatic substitution overview

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.[2]

This reaction type was discovered in 1970 by Bunnett and Kim [3] and the abbreviation SRN1 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[edit]

Radical-nucleophilic aromatic substitution 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:

AryneReaction Bunnett 1970

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:

Radical-nucleophilic aromatic substitution Bunnett 1970

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.[4]

References[edit]

  1. ^ Phenomenon of radical anion fragmentation in the course of aromatic SRN reactions Roberto A. Rossi Acc. Chem. Res.; 1982; 15(6) pp 164 - 170; doi:10.1021/ar00078a001.
  2. ^ Rossi, R. A.; Pierini, A. B.; Santiago, A. N. Org. React. 1999, 54, 1. doi:10.1002/0471264180.or054.01
  3. ^ Evidence for a radical mechanism of aromatic "nucleophilic" substitution Joseph F. Bunnett and Jhong Kook Kim J. Am. Chem. Soc.; 1970; 92(25) pp 7463 - 7464. (doi:10.1021/ja00728a037)
  4. ^ Alkali metal promoted aromatic "nucleophilic" substitution Joseph F. Bunnett and Jhong Kook Kim J. Am. Chem. Soc. 1970, 92, 7464 - 7466. (doi:10.1021/ja00728a038)

See also[edit]