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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1614675생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1614675

반응식

참여 물질

역할이름HCID투입량
반응물1-IodopentaneHCID 12335—
반응물2-(t-Butylsulfonamido)thiopheneHCID 19789655—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물2-Pentyl-5-(t-butylsulfonamido)thiopheneHCID 1893892160%

반응 조건

온도-20 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05198438
출처 데이터셋uspto-grants-1993_03
ORD IDord-3a87e448f60d4a7197645859f090430f
출처 메모uspto-grants-1993_03