A Further Investigation of the Symmetrical Chloride of Paranitroorthosulphobenzoic AcidHenderson, William Edwards
Science
A Further Investigation of the Symmetrical Chloride of Paranitroorthosulphobenzoic Acid
Henderson, William Edwards
Ortho-sulfobenzoic acid; Thesis (Ph. D.)
C=N.C₆H₅
/ \
/ .N.C₆H₅
/ /
Cal. for C₆H₃——SO₂
\
NO₂
Found.
I II III IV V
C = 60.11 59.47 59.93 —— —— ——
H = 3.44 3.69 3.82 —— —— ——
S = 8.45 —— —— 8.70 8.52 ——
N = 11.08 —— —— —— —— 11.35
For analyses I & II I am indebted to Mr. Nakaseko, who kindly made them
for me.
X. The Action of Reagents upon the Dianil of
Paranitroorthosulphobenzoic Acid.
1. The Action of Hydrochloric Acid on the Dianil
When the dianil is boiled for some time with concentrated hydrochloric
acid, the yellow color of the substance disappears, and the dianil is
converted into a colorless substance without, however, passing into
solution. The substance so obtained was filtered off, and crystallized
from alcohol. It crystallized in small colorless needles, which melted
at 183°, and possessed all the properties of the anil, which, in fact,
it proved to be. The reaction was therefore
C=N.C₆H₅ CO
/ \ / \
/ N.C₆H₅ / N.C₆H₅
/ / / /
C₆H₃——SO₂ + HCl + H₂O = C₆H₃——SO₂ + C₆H₅NH₃Cl
\ \
NO₂ NO₂
This reaction also explains the fact that some anil was always obtained
in making the dianil from the anilid. Hydrochloric acid is formed
in the reaction, and in turn acts on the dianil in the sense of the
equation just given.
2. The Action of Alcoholic Potash on the Dianil.
On boiling the dianil with alcoholic potash for a time, the solution
turned red, and nothing but tarry products were obtained. In this
respect the dianil differs from the dianil of orthosulphobenzoic acid,
which under similar conditions, is transformed into infusible anilid.
This observation is, however, in keeping with the fact that the nitro
derivative, is in general much less stable in the presence of alkali.
3. The Action of Glacial Acetic Acid on the Dianil.
When the dianil is boiled with glacial acetic acid for some time, the
color of the solution changes to a much lighter shade of yellow, or
becomes colorless. On evaporating the solution to small volume, and
allowing it to cool, a colorless substance separates. This is infusible
anilid. It could not be obtained in crystals from any solvent, but
always separated in flakes. It does not melt or undergo change at 340°.
Public-domain text, read in full here on John Shaqi.
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