CO / \ COCl / N.NH₄ / / / C₆H₃——SO₂Cl + 4NH₃ = C₆H₃——SO₂ + 2NH₄Cl. \ \ NO₂ NO₂ It was found that working in this way the symmetrical chloride could be prepared in pure condition, free from its isomer. The chloroform completely evaporates in a short time leaving fine crystals of the symmetrical chloride. In case the evaporation is slow and incomplete, it may be concluded that not all of the unsymmetrical chloride has been removed. The yield was uniformly about 40 per cent of the theoretical. From the water used to wash the chlorides a considerable amount of the original salt can be recovered, as the reaction under the conditions employed, is never complete. An examination was made of the substance mentioned as separating in the chloroform solution of the chlorides, during the treatment with ammonia, and it was found to possess the following properties. It is insoluble in benzene, chloroform, acetone, ether and ligroin; soluble in glacial acetic acid, from which it separates on cooling in colorless, crystalline condition; insoluble in the cold in water, alcohol and ammonia, but by boiling with these reagents, or by long standing in the cold, it is dissolved with decomposition. It was dissolved in hot water and the solution, which was acid in reaction, was neutralized with potassium carbonate. On adding an excess of hydrochloric acid to the solution, and allowing it to cool, characteristic crystals of acid potassium salt of paranitroorthosulphobenzoic acid separated. These properties identify the substance as the anhydride of this acid. The formation of the corresponding anhydride of orthosulphobenzoic acid by the action of phosphorus pentachloride upon its acid potassium salt was observed by Sohon[13], who made use of the reaction to prepare this anhydride in quantity. [13] Inaug. Diss. J. H. Univ. 1896. IV. Properties of the Symmetrical Chloride of Paranitroorthosulphobenzoic Acid. As first obtained, the crystals of the symmetrical chloride resemble irregularly shaped pieces of amber, both in color, and in lustre. On recrystallization from chloroform or ether, they may be obtained perfectly colorless, and are often of very simple crystallographic form. The chloride crystallizes in the monoclinic system, and possesses a very remarkable crystallizing power, in which respect it differs noticeably form its isomer. Even in chloroform solution that is far from dry, crystals appear with the greatest ease.