Electrolysis of phenyl and benzyl quaternary ammonium salts
โ Scribed by M. Finkelstein; R.C. Petersen; S.D. Ross
- Publisher
- Elsevier Science
- Year
- 1965
- Tongue
- English
- Weight
- 338 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0013-4686
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โฆ Synopsis
Electrolysis of the following salts in various solvents at an aluminum cathode gave benzene as the major cleavage product: trimethylanilinium nitrate, trimethylanilinium methoxide, triethylanilinium nitrate and triethylanilinium methoxide. The rate of formation of benzene was studied in several cases. Electrolysis of benzyltriethylammonium ion in dimethylformamide gave both toluene and bibenzyl while the electrolysis of benzyldimethylanilinium ion gave bibenzyl, toluene and benzene.
R&urn&-Son taux de formation d¬e que le benzene est le produit predominant, en solvants trts divers, du clivage Clectrolytique sur cathode Al, des sels suivants: anilinium; nitrate ou m6thoxyde de triCthylanilinium.
nitrate ou methoxyde de trimCthyl-Dans la formaldkhyde, l'ion benzyltri&thylammonium fournit conjointement du toluene et du dibenzyle, tandis que l'ion benzyldimethylammonium foumit en outre du benzkne.
๐ SIMILAR VOLUMES
Several good methods are known for the monodealkylation of quaternary ammonium compounds employing non-reductive nucleophilic agents (l-5). We wish to report here a simple one-step method that leads directly from a quaternary ammonium salt to the acyl derivative of the corresponding secondary amine
## Abstract The preparation and the physical properties of some quaternary ammonium salts are described.