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HRID 233194作成日:2026年10月26日

1,4-Dibromobutane → 4-(4-Bromobutyl)-1-(1,3-dithian-2-yl)ethylbenzene

https://huagongshe.com/reaction/233194

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DibromobutaneHCID 8056—
反応物Ethyl AcetateHCID 8857—
反応物4-Bromo-1-(1,3-dithian-2-yl)ethylbenzeneHCID 21960112—
反応物CID 53628100HCID 178418400—
溶媒TetrahydrofuranHCID 8028—
生成物4-(4-Bromobutyl)-1-(1,3-dithian-2-yl)ethylbenzeneHCID 21960129—

反応手順

A solution of 4-bromo-1-(1,3-dithian-2-yl)ethylbenzene (27.2 g, 94 mmol) in tetrahydrofuran (200 ml) was charged with sec-butyllithium (99 ml, 1.3M in cyclohexane, 0.13 mole) dropwise at -78° C. under nitrogen. The mixture was stirred at ambient temperature for 1.5 hours, and then quenched with 1,4-dibromobutane (42 g, 0.2 mole). After being stirred for 3 hours, the mixture was poured into ethyl acetate, and then washed with water and brine. The organic solution was then dried (Na2SO4) and concentrated to an oil. The crude product was purified by flash chromatography over a silica gel column. The 4-(4-bromobutyl)-1-(1,3-dithian-2-yl)-ethylbenzene thus purified was a light oil, 22.3 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05591745
出典データセットuspto-grants-1997_01
ORD IDord-02652182e58d43d2b42ef829bc3f9bc0
出典メモuspto-grants-1997_01