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A. I. Ilovaisky V. M. Merkulova Yu. N. Ogibin G. I. Nikishin 《Russian Chemical Bulletin》2005,54(7):1585-1592
Electrolysis of salts of primary and secondary nitro compounds (nitroethane, 1- and 2-nitropropanes, nitrocyclohexane, and
nitrocycloheptane) in the presence of excess halide, nitrite, cyanide, and phenylsulfinate anions under undivided and divided
amperostatic electrolysis conditions in a two-phase medium (CH2Cl2/H2O) produces geminal nitrohalides (35–85% yields), dinitro compounds (15–51%), nitronitriles (6–27%), and nitrosulfones (50–70%).
The salts of secondary nitro compounds form the products of oxidative coupling with halide and phenylsulfinate anions under
the undivided electrolysis conditions. In all other cases, divided electrolysis is required.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1539–1546, July, 2005. 相似文献
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