Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

Iodination of N-Methylquinolinuim salts

JB Daams, J Cymerman-Craig, C Ralph and D Willis

Australian Journal of Chemistry 8(3) 392 - 402
Published: 1955

Abstract

Iodination of N-methylquinaldinium iodide gives N-methylquinaldinium tri-iodide which with silver nitrate affords quinoline-2-aldehyde methiodide. A possible mechanism is advanced. Iodination of N-methyl-lepidinium iodide similarly yields N-methyl-lepidinium tri-iodide, but in this case silver nitrate treatment gives no aldehyde. Excess of iodine results in the diamagnetic bis(N-methyl-lepidinium)octa-iodide. The evidence obtained from absorption spectra and electrical conductivity measurements regarding ionic and intraionic dissociation of N-methylquinolinium polyiodides is discussed.

https://doi.org/10.1071/CH9550392

© CSIRO 1955

Committee on Publication Ethics


Export Citation Get Permission

View Dimensions