History of Chemistry, Volume 2 (of 2): From 1850 to 1910Thorpe, T. E. (Thomas Edward)
History
History of Chemistry, Volume 2 (of 2): From 1850 to 1910
Thorpe, T. E. (Thomas Edward)
Chemistry -- History
The artificial essence of violets known as _ionone_, prepared by
Tiemann in 1893, and now made commercially, is similar but not
identical in structure with the true perfume—_irone_. What is known as
_artificial musk_ is a trinitro-butyl toluol. _Artificial orange-flower
oil_ is a methyl ester of anthranilic acid.
In Vol. I. a short account has been given of the early history of
the large and important group of vegetable products known as the
_alkaloids_. Many of these have long been valued on account of their
powerful physiological action. As they all contain nitrogen and are
generally basic, they were regarded by Berzelius, and subsequently
by Liebig and Hofmann, as akin to ammonia in constitution, and were
classed as amines. The first experimental evidence of their nature
was obtained by Gerhardt, who found that, when strychnine and certain
of the alkaloids belonging to the quinine group are treated with
potash, an oil was obtained which he termed _quinoline_, and which was
recognised by Hofmann as identical with a substance obtained in 1834
from coal-tar by Runge, and at that time known as _leucol_. By other
modes of treatment certain alkaloids—_e.g._, nicotine and conine—are
found to yield pyridine, a basic substance found by Anderson, in 1846,
in the fœtid liquor obtained by distilling bones, and since found in
coal-tar. Others of them—_e.g._, papaverine, narcotine, etc.—yield
_isoquinoline_, an oil also discovered in coal-tar, by Hoogewerff, and
Van Dorp, in 1885. These three substances—quinoline, _iso_quinoline,
and pyridine—constitute so many nuclei in the constitution of a large
number of alkaloids. Pyridine resembles benzene in being a cyclic
compound, consisting of five carbon atoms and one nitrogen atom.
Quinoline stands to pyridine in much the same relation that naphthalene
stands to benzene. It can be obtained synthetically, as first shown by
Koenigs and Skraup, and subsequently by Doebner and Von Miller, from
benzene derivatives.
_Iso_quinoline, isomeric with quinoline, differs from that substance
in the position of the nitrogen atom. It, too, has been synthetically
prepared from benzene derivatives in a number of ways.
Public-domain text, read in full here on John Shaqi.
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