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HRID 234325作成日:2026年10月27日

Chlorosulfonic acid → 3-methoxythiophene-2-sulfonyl Chloride

https://huagongshe.com/reaction/234325

反応式

関与物質

役割名称HCID仕込み量
反応物Chlorosulfonic acidHCID 24638—
反応物Phosphorus oxychlorideHCID 24813—
反応物Phosphorus pentachlorideHCID 24819—
反応物3-MethoxythiopheneHCID 140249—
溶媒ChloroformHCID 6212—
生成物3-methoxythiophene-2-sulfonyl ChlorideHCID 1129882243.4%

反応条件

温度0 °C

反応手順

Chlorosulfonic acid (ClSO3H, 2.31 g, 19.62 mmol) was slowly added to a solution of 3-methoxythiophene (2.29 g, 19.62 mmol) in CHCl3 (80 ml) at 0° C. 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05594021
出典データセットuspto-grants-1997_01
ORD IDord-6c13f4bb83c240199d4200c43fc9398a
出典メモuspto-grants-1997_01