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IV.—On the Action of the Halogen Compounds of Ethyl and Amyl on some Vegetable Alkaloids

Published online by Cambridge University Press:  17 January 2013

Henry How
Affiliation:
Assistant to Professor Anderson, Glasgow University.

Extract

The memoir which I have now the honour of presenting to the Society contains part of a continued investigation, of which the first results were published in a paper read, last year, before the Chemical Society of London. The nature of the materials experimented on is such, and the scope of the subject so large, as to afford nothing more to all I have at present brought to light than the name of a bare and partial outline; yet the facts I have now to adduce, of some interest in themselves, will increase that of those already made known, and prove of additional service in aiding to complete that desirable object, a knowledge of the chemical constitution of the natural bases. In the paper alluded to, I shewed that, by the action of iodide of ethyl and of methyl upon morphia and codeine, the two most prominent alkaloids of opium, new salts are produced, in which the basic molecules appear to assimilate by their chemical characters to the hypothetical metal ammonium, or its oxide rather; so that, in the system of Hofmann, these peculiar results of natural, and as yet inimitable agencies, would take rank among the nitryle bases.

Type
Transactions
Copyright
Copyright © Royal Society of Edinburgh 1857

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References

page 27 note * Quart. Journ. Chem. Soc, vol. vi.

page 28 note * Trans. Roy. Soc. Edin., vol. xxi., part i.

page 29 note * Quart. Journ. Chem. Soc, vol. vi.

page 30 note * Loc. cit.

page 31 note * Journal für Praktische Chemie, vol. liii., p. 431; Chem. Gazette, 1852, p. 36.

page 32 note * Gerhardt Suite de Berzelius, ii., p. 323.

page 39 note * Liebig. Traité de Chimie Organique, par Gerhardt ii., p. 630.

page 40 note * Chemical Gazette, 1853, p. 470.