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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 375194생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/375194

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfenyl chloride, trifluoro-HCID 67900—
반응물ethyl 4-(4-chlorophenyl)-1H-pyrrole-3-carboxylateHCID 470434—
용매DichloromethaneHCID 6344—
생성물Ethyl 4-(p-chlorophenyl)-5-[(trifluoromethyl)thio]pyrrole-3-carboxylateHCID 1893038995.3%

반응 조건

온도-30 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05484807
출처 데이터셋uspto-grants-1996_01
ORD IDord-e21a252a88244b3a9d0b69f9180d2ee6
출처 메모uspto-grants-1996_01