Meta toluene sulphonic acid and related compounds — John Shaqi
Meta toluene sulphonic acid and related compoundsAllen, C. F. H. (Charles Francis Hitchcock)
Science
Meta toluene sulphonic acid and related compounds
Allen, C. F. H. (Charles Francis Hitchcock)
Organic compounds -- Synthesis; Sulfonic acids
The object of this paper is to prepare a solution of meta toluene
sulphonic acid, as probably obtained by Griffin, by the most promising
of the investigated methods and to find an acceptable one for isolating
the acid in the solid state. After a solution is obtained similar to
that found by Griffin, (loc. cit.), the intention is to remove as much
water as possible by distillation under diminished pressure and then
to precipitate the acid by the method of Kastle, (Amer. Chem. J., Vol.
44, page 483), namely saturate the remaining solution with gaseous
hydrochloric acid. It is hoped that in this way the solid acid may be
obtained which can then be studied.
As has been proved by previous experimenters and discussed above,
no direct method of sulphonating toluene will give any of the meta
sulphonic acid. Therefore to get a compound containing a methyl group
with a sulphonic acid group in the position meta to it some compound
with these already in that position and containing some other group
which can be replaced by hydrogen might be used, i.e. a disubstituted
toluene. The two groups which can be readily replaced by hydrogen are
the amino group and bromine, the former by the diazo reaction and
the latter by treatment with metallic sodium; the easier of the two
to prepare and replace is the amino group and this is the one made
use of in this synthesis. This replacement has been widely studied
(Amer. Chem. J., by Palmer 8, 243; Orndorff 9, 387; Graham 11, 319;
Dashiell 15, 124; Metcalf 15, 301; Parks 15, 320; Shober 15, 379;
Beeson 16, 244; and Dissertations by Weida, Cameron, and Chamberlain,
all 1894.), and the various conditions affecting it determined. The
foregoing investigators decomposed their diazo compounds with alcohols
sometimes using certain substances to cause the alkoxy or hydrogen
reactions to take place. Later investigators (Buchka, Berichte 23,
1628, St. Von Niemantowski, Ibid., 34, 3325 (1901), Ullman and Bieleck,
Ibid., 34, 2174, and Bigelow, J. Amer. Chem. Soc., Vol. 41, 1566), have
shown that this decomposition is greatly increased by the presence of
copper powder. As the first method has been more extensively studied it
was adopted in this case.
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