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735834 
Journal Article 
One-step synthesis of carbon-sulphur heterocyclic ring by electrochemical reduction of carbon disulphide at platinum electrode 
Srivastav, MK; Saraswat, A; Sharma, LK; Singh, RKP 
2010 
Yes 
Journal of the Indian Chemical Society
ISSN: 0019-4522 
87 
1131-1135 
English 
The electro reductive cyclization of carbon disulphide in nonaqueous solvent is reported here. At constant potential, the electrolysis of carbon disulphide was carried out in the presence of an electrophile i.e. alkyl cation, acyl cation etc. using N/N-dimethylformamide, acetonitrile or DMSO as a nonaqueous solvent and tetrabutylammonium iodide, tetraethylammonium phosphate as a supporting electrolyte. Electro reductive cyclization of carbon disulphide gives 4,5-disubstituted thio-1,3-dithiole-2-thione at platinum cathode. This is a one pot electrochemical synthesis which takes place at room temperature. 
Carbon disulphide; Electrochemical reduction; Platinum electrode; Synthesis