Org. Synth. 1942, 22, 70
DOI: 10.15227/orgsyn.022.0070
IODOSOBENZENE
[Benzene, iodoso-]
Submitted by H. J. Lucas, E. R. Kennedy, and M. W. Formo.
Checked by Lee Irvin Smith, R. T. Arnold, and R. A. Matthews.
1. Procedure
In a
large mortar chilled in an
ice bath are placed
55 g. (0.2 mole) of iodobenzene dichloride (p. 482),
50 g. of anhydrous sodium carbonate, and 100 g. of finely crushed ice. The mixture is ground thoroughly
(Note 1) until all the ice has melted and a thick paste results. To this suspension
140 ml. of 5 N sodium hydroxide is added, in 20-ml. portions, with repeated trituration after each addition. Finally, 100 ml. of water is added to render the mixture more fluid and the material is allowed to stand overnight. The product is collected with suction, pressed thoroughly on the filter, transferred to a
beaker, and washed thoroughly with 300 ml. of water
(Note 2). The material is filtered with suction, washed again in a beaker with 300 ml. of water, collected with suction, and washed with about 250 ml. of water on the filter. After thorough drying in the air, the product is stirred to a thin mush with a little
chloroform (Note 3), freed of solvent by suction, and spread on filter paper to dry in the air. The yield is
26–27 g. (
60–62%) of a product having a purity of about 99%, as determined by titration
(Note 4) and
(Note 5).
2. Notes
1.
The solid forms a caked mass, which is disintegrated by trituration.
2.
The filtrate contains some diphenyliodonium salts, which may be recovered in the form of the sparingly soluble iodide by the addition of
potassium iodide (p. 355). Usually
7–9 g. of diphenyliodonium iodide is obtained.
3.
The
chloroform removes
iodobenzene, which may be recovered.
4.
The following procedure is used in the analysis of iodoso and iodoxy compounds. In a
200-ml. iodine flask are placed 100 ml. of water,
10 ml. of 6 N sulfuric acid,
2 g. of iodate-free potassium iodide,
10 ml. of chloroform, and finally the sample, about 0.25 g. The flask is shaken for 15 minutes (or longer, if the reaction is not complete), and then the mixture is titrated with
0.1 N sodium thiosulfate. If the sample is pure the change of color in the
chloroform layer may be taken as the end point, but if impurities are present starch must be used, for the impurities impart a brownish color to the
chloroform. This solvent is desirable, as it facilitates the reaction with
potassium iodide by dissolving the reaction products.
Iodosobenzene may be differentiated from
iodoxybenzene, for the former reduces iodide ion in a saturated
sodium borate solution, whereas the latter does not.
1 The reactions involved are:
C
6H
5IO + 2HI → C
6H
5I + H
2O + I
2
C
6H
5IO
2 + 4HI → C
6H
5I + 2H
2O + 2I
25.
For use in the preparation of
iodoxybenzene by the disproportionation method
(p. 485) it is superfluous to dry the crude product and to wash it with
chloroform to remove
iodobenzene. The crude wet
iodosobenzene may also be used directly for the preparation of
diphenyliodonium iodide (p. 355), but it is desirable to assay the wet product by titration to determine the quantity of
iodoxybenzene needed.
3. Discussion
Iodosobenzene has been prepared by the action of aqueous
sodium or potassium hydroxide upon
iodobenzene dichloride;
2 and by repeated additions of water to
iodobenzene dichloride.
3
This preparation is referenced from:
Appendix
Chemical Abstracts Nomenclature (Collective Index Number);
(Registry Number)
sodium or potassium hydroxide
sulfuric acid (7664-93-9)
sodium hydroxide (1310-73-2)
chloroform (67-66-3)
sodium carbonate (497-19-8)
potassium iodide (7681-11-0)
sodium thiosulfate (7772-98-7)
Iodobenzene (591-50-4)
iodobenzene dichloride (2401-21-0)
DIPHENYLIODONIUM IODIDE (2217-79-0)
Iodosobenzene,
Benzene, iodoso- (536-80-1)
Iodoxybenzene (696-33-3)
sodium borate
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