The oxidation of arylacetic acids by peroxydisulphate in acetic acid media in the presence of potassium and copper-(II) acetates leads to the corresponding benzylacetates. The mechanism of the reaction is rationalized by the occurrence of two pathways: the intermediate formation of aromatic radical cations or the direct decarboxylation of the arylacetate ion. The importance of acetic acid as a rection medium is stressed.

Electron-transfer processes: oxidation of arylacetic acids by peroxydisulphate in acetic acid

Citterio, Attilio;Minisci, Francesco
1981-01-01

Abstract

The oxidation of arylacetic acids by peroxydisulphate in acetic acid media in the presence of potassium and copper-(II) acetates leads to the corresponding benzylacetates. The mechanism of the reaction is rationalized by the occurrence of two pathways: the intermediate formation of aromatic radical cations or the direct decarboxylation of the arylacetate ion. The importance of acetic acid as a rection medium is stressed.
1981
Chimica Organica, Free Radicals, Oxidation, Peroxydisulfate, Aromatic Radical Cation
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11311/1047403
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