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HRID 129638作成日:2026年10月27日

1,2-Dichloroethane → 2-(p-Chlorophenyl)-3-[(trifluoromethyl)sulfonyl]-5-[(trifluoromethyl)thio]pyrrole

https://huagongshe.com/reaction/129638

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物Trifluoromethanesulfonic acidHCID 62406—
反応物Methanesulfenyl chloride, trifluoro-HCID 67900—
反応物2-(p-Chlorophenyl)-3-[(trifluoromethyl)sulfonyl]pyrroleHCID 10448068—
溶媒DichloromethaneHCID 6344—
生成物2-(p-Chlorophenyl)-3-[(trifluoromethyl)sulfonyl]-5-[(trifluoromethyl)thio]pyrroleHCID 1893040672%

反応条件

温度70 °C

反応手順

A solution of 2-(p-chlorophenyl)-3-[(trifluoromethyl)sulfonyl]pyrrole (2.47 g, 0.0080 mol), trifluoromethylsulfenyl chloride (2.18 g, 0.016 mol), trifluoromethanesulfonic acid (0.12 g, 0.0008 mol) and 1,2-dichloroethane (15 mL) is placed in a pressure tube, heated at 70° C. for five days, diluted with methylene chloride, washed with saturated sodium hydrogen carbonate solution and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to obtain an amber syrup. Flash chromatography of the syrup using silica gel and a 1:5 ethyl acetate/hexanes solution gives the title product as an off-white solid (2.36 g, mp 118°-122° C.) which is identified by 1HNMR and 13CNMR spectral analyses.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05468877
出典データセットuspto-grants-1995_11
ORD IDord-266616786e864f3889254a00732a3a34
出典メモuspto-grants-1995_11