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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 232755생성일: 2026년 10월 26일

Chlorosulfonic acid → 3-methoxythiophene-2-sulfonyl Chloride

https://huagongshe.com/reaction/232755

반응식

참여 물질

역할이름HCID투입량
반응물Chlorosulfonic acidHCID 24638—
반응물Phosphorus oxychlorideHCID 24813—
반응물Phosphorus pentachlorideHCID 24819—
반응물3-MethoxythiopheneHCID 140249—
용매ChloroformHCID 6212—
생성물3-methoxythiophene-2-sulfonyl ChlorideHCID 1129882243.4%

반응 조건

온도0 °C

반응 단계

Chlorosulfonic acid (ClSO3H, 2.31 g, 19.62 mmol) was slowly added at 0° C. to a solution of 3-methoxythiophene (2.29 g, 19.62 mmol) in CHCl3 (80 ml) The resulting mixture was stirred at 0° C. for 30 min. The solvent was evaporated under reduced pressure, at room temperature, the residue was suspended in POCl3 (15 ml, 156.96 mmol), and PCl5 (8.2 g, 39.24 mmol) was added slowly. The reaction was stirred at 60° C. for 18 h, then cooled to room temperature and poured onto crushed ice (200 g). The aqueous mixture was extracted with CHCl3 (2×150 ml) and the combined organic layers was dried (MgSO4). The solid was removed by filtration and the filtrate was concentrated to give 3-methoxy-2-thiophenesulfonyl chloride as a brown oil (1.81 g, 43% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05591761
출처 데이터셋uspto-grants-1997_01
ORD IDord-260f0f7ab5354dafbb23a5e3d06e44bd
출처 메모uspto-grants-1997_01