An ortho-directing effect in the nucleophilic aromatic substitution reactions of primary and secondary 2,4-dichloro- and 2,3,4-trichlorobenzamides with ethanethiolate

Article abstract of DOI:10.1080/00397919508013427

The reactions of the primary amide and several secondary amides of 2,4-dichloro- and 2,3,4-trichlorobenzoic acid with potassium ethanethiolate in DMF were observed to proceed with a remarkable degree of ortho-regioselectivity. This effect was found to be

Full text of DOI:10.1080/00397919508013427

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Synthetic Communications: An
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Organic Chemistry
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An Ortho-Directing Effect in
the Nucleophilic Aromatic
Substitution Reactions of
Primary and Secondary
2,4-Dichloro- and 2,3,4-
Trichlorobenzamides with
Ethanethiolate
Geoffrey K. Cooper a , Don R. Baker a & Larry B.
Barden a
a Western Research Center, Zeneca Agricultural
Products , Richmond, California, 94804
Published online: 23 Sep 2006.
To cite this article: Geoffrey K. Cooper , Don R. Baker & Larry B. Barden (1995) An
Ortho-Directing Effect in the Nucleophilic Aromatic Substitution Reactions of Primary
and Secondary 2,4-Dichloro- and 2,3,4- Trichlorobenzamides with Ethanethiolate,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 25:6, 899-906, DOI: 10.1080/00397919508013427
To link to this article: http://dx.doi.org/10.1080/00397919508013427
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