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HRID 375194作成日:2026年10月26日

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

https://huagongshe.com/reaction/375194

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US05484807
出典データセットuspto-grants-1996_01
ORD IDord-e21a252a88244b3a9d0b69f9180d2ee6
出典メモuspto-grants-1996_01