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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Antimony trichloride | HCID 24814 | — |
| Edukt | (Bis(2-methoxyethyl)amino)sulfur trifluoride | HCID 2734690 | — |
| Edukt | 2-Methyl-5-[3-[4-(methylthio)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazole | HCID 44481756 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-[3-[4-[(Fluoromethyl)thio]phenyl]-1-benzofuran-5-yl]-5-methyl-1,3,4-oxadiazole | HCID 68663962 | 30,4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08492378B2 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-f89e108746f840ab95f83b7d38c22bb8 |
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| Quellennotiz | uspto-grants-2013_07 |
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