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1998 carboxylic acids carboxylic acids (benzene compounds) Q 0420 18 - 102 Selective Oxidation of Substituted Xylenes to Toluic Acids by Hypochlorite–Ru System under Phase - Transfer Conditions. Under phase-transfer conditions the reactant is transferred to the aqueous phase as the sodium salt of the benzoic acid immediately after the oxidation of the methyl group. Thus, only one of the two methyl groups is oxidized. Unsubsti- tuted xylene or xylenes bearing electron-donating groups form ring-chlorinated products together with some side chain chlorinated products. — (SASSON, Y.; AL QUNTAR, A. E.-A.; ZORAN, A.; Chem. Commun. (Cambridge) (1998) 1, 73-74; Casali Inst. Appl. Chem., Sch. Appl. Sci. Technol., Hebrew Univ., Jerusalem 91904, Israel; EN) 1

ChemInform Abstract: Selective Oxidation of Substituted Xylenes to Toluic Acids by Hypochlorite—Ru System under Phase - Transfer Conditions

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Page 1: ChemInform Abstract: Selective Oxidation of Substituted Xylenes to Toluic Acids by Hypochlorite—Ru System under Phase - Transfer Conditions

1998 carboxylic acids

carboxylic acids (benzene compounds)Q 0420

18 - 102Selective Oxidation of Substituted Xylenes to Toluic Acids byHypochlorite–Ru System under Phase - Transfer Conditions. —Under phase-transfer conditions the reactant is transferred to the aqueous phaseas the sodium salt of the benzoic acid immediately after the oxidation of themethyl group. Thus, only one of the two methyl groups is oxidized. Unsubsti-tuted xylene or xylenes bearing electron-donating groups form ring-chlorinatedproducts together with some side chain chlorinated products. — (SASSON,Y.; AL QUNTAR, A. E.-A.; ZORAN, A.; Chem. Commun. (Cambridge) (1998)1, 73-74; Casali Inst. Appl. Chem., Sch. Appl. Sci. Technol., Hebrew Univ.,Jerusalem 91904, Israel; EN)

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