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HRID 1625849作成日:2026年10月25日

1,1-Dibromoethane → Tributyl-(4-ethylphenyl)stannane

https://huagongshe.com/reaction/1625849

反応式

関与物質

役割名称HCID仕込み量
反応物1,1-DibromoethaneHCID 11201—
反応物Tributyltin ChlorideHCID 15096—
反応物1-Bromo-4-ethylbenzeneHCID 15313—
反応物Potassium FluorideHCID 522689—
反応物MagnesiumHCID 5462224—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物Tributyl-(4-ethylphenyl)stannaneHCID 6004126792.9%

反応手順

To a solution of magnesium (896 mg) in tetrahydrofuran (20 ml) was added dibromoethan (0.1 ml), and the mixture was stirred at room temperature for 15 minutes. Thereto was added dropwise a solution of 1-bromo-4-ethylbenzene (5.7 g) in tetrahydrofuran (20 ml), and subsequently, the mixture was stirred at room temperature for one hour. The reaction mixture was cooled to −78° C., and thereto was added dropwise tributyltin chloride (9.49 g). The mixture was stirred at the same temperature for 30 minutes, and then at room temperature for one hour. To the reaction mixture were added 10% aqueous potassium fluoride solution and ethyl acetate, and the mixture was stirred at room temperature for 30 minutes. Insoluble materials were filtered off. The organic layer of the filtrate was washed with water and brine successively, and dried over sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by alumina column chromatography (hexane) to give the desired tri-n-butyl(4-ethylphenyl)tin (10.7 g) as colorless oil. EI-Mass m/Z 337 (M-Bu).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08785403B2
出典データセットuspto-grants-2014_07
ORD IDord-99bc2f8f412b49c5965786b6e664c47f
出典メモuspto-grants-2014_07