Facile and one-pot,electro-organic synthesis of a new bis-quinone by the ECCE mechanism in green med

来源 :Chinese Chemical Letters | 被引量 : 0次 | 上传用户:sz398143634
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Electrochemical oxidation of 4-methyl catechol(1a) is investigated in the presence of 1,3-indandione(3)as nucleophile in phosphate buffer solution(0.2 mol/L,pH 6) mixed with ethanol as organic green solvent(50/50) using cyclic voltammetry and controlled-potential coulometry.The results indicated thatquinones derived from electro-oxidation of 1a,participated in a 1,4-Michael addition reaction with1,3-indandione(3) under ECCE mechanism.In this direction,a new bis-quinone was synthesized in high yield and good purity using a facile and convenient electrochemical pathway by carbon anode electrodes in an undivided cell. Electrochemical oxidation of 4-methyl catechol (1a) was investigated in the presence of 1,3-indandione (3) as nucleophile in phosphate buffer solution (0.2 mol / L, pH 6) ) using cyclic voltammetry and controlled-potential coulometry. The results indicated that quinones derived from electro-oxidation of 1a, participated in a 1,4-Michael addition reaction with 1,3-indandione (3) under ECCE mechanism. bis-quinone was synthesized in high yield and good purity using a facile and convenient electrochemical pathway by carbon anode electrodes in an undivided cell.
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