6533b86cfe1ef96bd12c7ef0

RESEARCH PRODUCT

STUDIEN ZUM VORGANG DER WASSERSTOFFÜBERTRAGUNG 621HERSTELLUNG UND ELEKTROREDUKTIVE SPALTUNG EINIGER ARYLDISULFONSÄUREDERIVATE

Rolf-erhard SchmittLeopold Horner

subject

chemistry.chemical_classificationchemistry.chemical_compoundElectrical currentchemistryFissionPhenolOrganic chemistryAlcoholAmine gas treatingMethanolSulfinic acidAcetonitrileMedicinal chemistry

description

Abstract Benzene-disulfonylchlorides were converted to the corresponding dialkyl-and diphenylesters, N-alkyl-and N-aryl disulfonamides. The half-wave-potentials E1/2 1 and E1/2 2 were measured and the products obtained on potentiostatic fission at E1/2 1 were isolated and characterized. The electroreduction of benzene-1,4-disulfonic acid-diphenylester in methanol yields phenol in a quantity approximately corresponding to the current passed, but no corresponding quantity of sulfinic acid. In dry acetonitrile, benzene-1,4-disulfonic acid diesters and diamides undergo potentiostatic fission (at E1/2 1) in good chemical and current yields, giving the corresponding monosulfonate-sulfinic acid or monosulfonamide-sulfinic acid and alcohol or amine. The passage of further electrical current reduces the sulfinic acids to other, as yet undetermined, products. Ausgehend von den Benzoldisulfonsauredichloriden werden die entsprechenden Dialkyl-und Diphenylester sowie Alkyl-und Aryldisulfonsaurediamide hergestellt. Die...

https://doi.org/10.1080/03086648208081175