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HRID 129636作成日:2026年10月27日

Methanesulfenyl chloride, trifluoro- → Ethyl 4-(p-chlorophenyl)-5-[(trifluoromethyl)thio]pyrrole-3-carboxylate

https://huagongshe.com/reaction/129636

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfenyl chloride, trifluoro-HCID 67900—
反応物ethyl 4-(4-chlorophenyl)-1H-pyrrole-3-carboxylateHCID 470434—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 4-(p-chlorophenyl)-5-[(trifluoromethyl)thio]pyrrole-3-carboxylateHCID 1893038995.3%

反応条件

温度-30 °C

反応手順

A solution of ethyl 4-(p-chlorophenyl)-pyrrole-3-carboxylate (9.0 g, 0.036 mol) in methylene chloride (180 mL) is treated with trifluoromethylsulfenyl chloride (4.9 g, 0.036 mol) with stirring for 45 minutes at -30° C. The reaction mixture is warmed to room temperature and stirred for several hours. Since a TLC shows some starting material present, the reaction mixture is cooled to -30° C., treated with additional trifluoromethylsulfenyl chloride (1.3 g, 0.0095 mol), warmed to room temperature overnight with stirring, washed with water, saturated sodium hydrogen carbonate solution and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to give the title product as an off-white solid (12.0 g, mp 161.5°-164.0° C.) which is identified by 1HNMR, 19FNMR 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-d828b9dc94e5433fa332716acebd0fc7
出典メモuspto-grants-1995_11