戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 366638作成日:2026年10月25日

(Diethylamino)sulfur trifluoride → 5-Fluoro-4-iodoindolin-2-one

https://huagongshe.com/reaction/366638

反応式

関与物質

役割名称HCID仕込み量
反応物(Diethylamino)sulfur trifluorideHCID 123472—
反応物1-Hydroxy-4-iodo-1,3-dihydro-indol-2-oneHCID 14740977—
溶媒DichloromethaneHCID 6344—
生成物5-Fluoro-4-iodoindolin-2-oneHCID 9795601—

反応条件

温度-25 °C

反応手順

A suspension of 1,3-dihydro-1-hydroxy-4-iodo-2H-indol-2-one, (2.43 g, 9 mmol) (see below) in dry dichloromethane (500 mL) was cooled to -25° C. under an argon atmosphere with magnetic stirring. A solution of (diethylamino)sulfur trifluoride (DAST, 1.35 mL) (Aldrich) in dry dichloromethane (40 mL) was added dropwise at such a rate that the reaction temperature did not rise above -25° C. (about 15 min.). After stirring for an additional 30 min. at -25° C., the reaction was quenched by the addition of saturated aqueous sodium bicarbonate solution (180 mL) and allowed to warm to room temperature. The mixture was then filtered through Celite® (Fisher Scientific) and the layers separated. The aqueous layer was extracted with dichloromethane (2×300 mL). The dichloromethane layers were washed with saturated aqueous sodium chloride solution (200 mL), combined, dried (magnesium sulfate) and concentrated. Residue was purified by flash chromatography on silics gel using ethyl acetate-dichloromethane (1:7, V/V) as solvent to give 1,3-dihydro-5-fluoro-4-iodo-2H-indol-2-one. (Yield 1.08 g, 43%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06130239
出典データセットuspto-grants-2000_10
ORD IDord-26728569763b487d9f1a456fb8febcdf
出典メモuspto-grants-2000_10