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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 129638Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/129638

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
EduktTrifluoromethanesulfonic acidHCID 62406—
EduktMethanesulfenyl chloride, trifluoro-HCID 67900—
Edukt2-(p-Chlorophenyl)-3-[(trifluoromethyl)sulfonyl]pyrroleHCID 10448068—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(p-Chlorophenyl)-3-[(trifluoromethyl)sulfonyl]-5-[(trifluoromethyl)thio]pyrroleHCID 1893040672%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05468877
Quelldatensatzuspto-grants-1995_11
ORD IDord-266616786e864f3889254a00732a3a34
Quellennotizuspto-grants-1995_11