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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 452782Erstellt: 24. Oktober 2026

Antimony trichloride → 2-[3-[4-[(Fluoromethyl)thio]phenyl]-1-benzofuran-5-yl]-5-methyl-1,3,4-oxadiazole

https://huagongshe.com/de/reaction/452782

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAntimony trichlorideHCID 24814—
Edukt(Bis(2-methoxyethyl)amino)sulfur trifluorideHCID 2734690—
Edukt2-Methyl-5-[3-[4-(methylthio)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazoleHCID 44481756—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-[3-[4-[(Fluoromethyl)thio]phenyl]-1-benzofuran-5-yl]-5-methyl-1,3,4-oxadiazoleHCID 6866396230,4%

Reaktionsschritte

To a solution of [bis(2-methoxyethyl)amino]sulfur trifluoride (1.38 mL, 7.50 mmol) in dichloromethane (10 mL) was added dropwise a solution of 2-methyl-5-[3-[4-(methylthio)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazole (1.61 g, 5.00 mmol) in dichloromethane (15 mL) at room temperature. Antimony (III) chloride (0.0570 g, 0.250 mmol) was added to the solution, and the resulting mixture was stirred overnight at room temperature. The reaction mixture was diluted with ethyl acetate, washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/tetrahydrofuran=1/1) and recrystallized from hexane/ethyl acetate to give the title compound (517 mg, yield 30%) as pale-yellow crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08492378B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-f89e108746f840ab95f83b7d38c22bb8
Quellennotizuspto-grants-2013_07