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Synthesis
To 87 g. (100 cc., 1.1 moles) of benzene in a 1-l. three-necked flask provided with a mechanical stirrer, is added 30 g. (0.22 mole) of anhydrous aluminum chloride. The suspension is cooled in an ice bath, and to it is added, with stirring, 40 g. (0.13 mole) of diphenylselenium dichloride in portions of approximately 1 g. at a time over a period of twenty-five minutes. Before each addition the temperature should be below 10° to prevent the final product from becoming dark. When the addition is complete, the reaction mixture is allowed to stand for three hours at room temperature, and then 200 cc. of water is added cautiously. The benzene layer is separated and discarded. If the water layer is colored, further extractions with benzene will remove most of the color without reducing the yield. The water layer is then extracted three times with 50-cc. portions of chloroform. The combined extracts are concentrated to a volume of 40 cc. and treated with 120 cc. of ether. A yellow oil precipitates and solidifies almost at once to a white powder. The triphenylselenonium chloride is collected on a filter and recrystallized from 300 cc. of methyl ethyl ketone to which 20 cc. of water has been added. The yield of anhydrous product, after drying at 100°, is 30 g.
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