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 Preparation of Diphenyl selenide
  • Preparation of Diphenyl selenide
  • Di (CAS NO.: ), which is also known as Phenyl selenide, could be produced through the following synthetic routes.

    Preparation of Diphenyl selenide

    In a 500-cc. beaker are placed 360 g. (6.4 moles) of powdered potassium hydroxide and 240 g. (3 gram atoms) of black powdered selenium which have been previously ground together in a mortar. This mixture is heated in an oil bath at 140–150° until a thick, dark red liquid is formed, and then it is added in small portions to 400 cc. of ice water in a 5-l. flask. The solution is kept in an ice bath until used.

    To 375 cc. (4.3 moles) of hydrochloric acid (sp. gr. 1.18) and 200 g. of ice is added 139.6 g. (1.5 moles) of aniline. The resulting solution is diazotized with a solution of 103.5 g. (1.5 moles) of c.p. sodium nitrite, ice being added to the reaction mixture, as necessary, in order to keep the temperature below 5°. The final volume of the diazotized solution is about 1 l. This solution is added in a slow stream from a dropping funnel to the potassium selenide solution, which is vigorously stirred with a mechanical stirrer. When all the diazotized solution has been added, the red aqueous solution is decanted from the dark oil which forms and is heated to boiling. It is then poured back on the oil, the mixture is well stirred, 200 cc. of chloroform is added, and the selenium is collected on a filter and washed with a little more chloroform. After the chloroform layer is separated, the aqueous layer is again extracted with 200 cc. of chloroform. The combined extracts are then distilled, the diphenyl selenide being collected from 300 to 315°. The yield of yellow oil of rather unpleasant odor is 138–150 g. (79–86 per cent of the theoretical amount). If a purer product is desired, this material can be distilled under diminished pressure. It boils at 165–167°/12 mm.


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