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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1464670생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1464670

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 mi) 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°-164.00° C.) which is identified by 1HNMR, 19FNMR and 13CNMR spectral analyses.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05306827
출처 데이터셋uspto-grants-1994_04
ORD IDord-dd9f1e78590346f9a21494eb23d5a77f
출처 메모uspto-grants-1994_04