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HRID 1277564作成日:2026年10月27日

Potassium Carbonate → Benzene, 1,1'-selenobis-

https://huagongshe.com/reaction/1277564

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Phenyl selenoxideHCID 305982—
触媒Osmium TetroxideHCID 30318—
溶媒AcetoneHCID 180—
生成物Benzene, 1,1'-selenobis-HCID 1433380%

反応手順

A 100 ml Fischer-Porter glass pressure reactor, equipped with a magnetic stirring bar was successively charged with 2.5 g (0.01 moles) of diphenylselenoxide, 10 ml acetone, 10 ml 0.1 N potassium carbonate solution, and 0.63 ml of an osmium tetroxide solution (4% OsO4 in 0.1 N K2CO3). The reactor was attached to a gas manifold, flushed with nitrogen and then pressurized with 80 psig ethylene. The mixture was magnetically stirred at room temperature for two hours until the reaction of the gaseous olefin ceased as evidenced by a constant gas pressure. Sodium bisulfate (5 ml of a 10 wt. % aqueous solution) was added to reduce both the remaining selenoxide and osmium tetroxide. The reaction mixture was transferred to a separatory funnel and the oily layer of diphenylselenide, formed during reaction, separated from the aqueous layer containing the solvent and glycol product. The wateracetone layer contained 0.49 g ethylene glycol (80% yield based on the amount of diphenylselenoxide used) as determined by gas chromatographic analysis.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04278517
出典データセットuspto-grants-1981_07
ORD IDord-daf5f5172c9f4e01a5504b8f58606341
出典メモuspto-grants-1981_07