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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1464673Erstellt: 24. Oktober 2026

Bromine → 3-Bromo-5-(p-chlorophenyl)-4-[(trifluoromethyl)sulfonyl]-2-[(trifluoromethyl)thio]pyrrole

https://huagongshe.com/de/reaction/1464673

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromineHCID 24408—
Edukt2-(p-Chlorophenyl)-3-[(trifluoromethyl)sulfonyl]-5-[(trifluoromethyl)thio]pyrroleHCID 18930406—
KatalysatorBromineHCID 24408—
LösungsmittelChloroformHCID 6212—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-Bromo-5-(p-chlorophenyl)-4-[(trifluoromethyl)sulfonyl]-2-[(trifluoromethyl)thio]pyrroleHCID 1893039041,9%

Reaktionsschritte

A solution of 2-(p-chlorophenyl)-3-[(trifluoromethyl)sulfonyl]-5-[(trifluoromethyl)thio]pyrrole (0.5 g, 0.00122 mol) in chloroform (10 mL) is cooled with an ice bath, treated with a solution of bromine (0.21 g, 0.00134 mol) in chloroform (5 mL), stirred for two hours, warmed to room temperature, treated with two drops of additional bromine and stirred for one hour. The reaction mixture is diluted with methylene chloride, washed with water, saturated sodium hydrogen carbonate solution, saturated sodium metabisulfite solution and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to obtain a syrup. Flash chromatography of the syrup using silica gel and a 1:5 ethyl acetate/hexanes solution gives the title product as a white solid (0.25 g, mp 122°-125° C.) which is identified by 1HNMR and 13CNMR spectral analyses.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05306827
Quelldatensatzuspto-grants-1994_04
ORD IDord-c24cdfa4d1f2413daed18bb5f6baad4f
Quellennotizuspto-grants-1994_04