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HRID 1614675作成日:2026年10月27日

1-Iodopentane → 2-Pentyl-5-(t-butylsulfonamido)thiophene

https://huagongshe.com/reaction/1614675

反応式

関与物質

役割名称HCID仕込み量
反応物1-IodopentaneHCID 12335—
反応物2-(t-Butylsulfonamido)thiopheneHCID 19789655—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物2-Pentyl-5-(t-butylsulfonamido)thiopheneHCID 1893892160%

反応条件

温度-20 °C

反応手順

To a solution of 2-(t-butylsulfonamido)thiophene (3.42 g, 15.6 mmol) in anhydrous THF coole to -78° C. under N2 was added 2.5M n-BuLi (15.6 mL, 2.5 equiv). The reaction was warmed to -20° C. over 3.5 h After stirring at -20° C. for an addional h, iodopentane (2.4 mL, 1.2 equiv) was added. The ice bath was removed and the reaction was stirred at rt overnight. The next day the reaction was quenched with sat'd NH4Cl solution and the THF was removed in vacuo. The residue was extracted with Et2O/EtOAc and washed with water and brine. The organic was dried over anhydrous MgSO4 and concentrated in vacuo. The product was purified by flash chromatography on a silica column eluting with Hex/EtOAc (15:1). Removal of the solvent afforded 2.72 g (60%) of the titled compound as a yellow oil. Rf=0.4 (6:1 Hex/EtOAc).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05198438
出典データセットuspto-grants-1993_03
ORD IDord-3a87e448f60d4a7197645859f090430f
出典メモuspto-grants-1993_03