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HRID 55629作成日:2026年10月25日

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

https://huagongshe.com/reaction/55629

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US05624927
出典データセットuspto-grants-1997_04
ORD IDord-cc86d0d5ecef4ee2a25a5d47c5f2118a
出典メモuspto-grants-1997_04