HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Carbon Disulfide → HCID 178506378, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Carbon Disulfide | HCID 6348 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 3-[3-(Trifluoromethoxy)phenyl]-1-benzofuran-5-carbohydrazide | HCID 68664388 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | HCID 178506378 | HCID 178506378 | — |
Reaktionsschritte
A mixture of the obtained 3-[3-(trifluoromethoxy)phenyl]-1-benzofuran-5-carbohydrazide, triethylamine (5.6 mL, 40.4 mmol), carbon disulfide (18.2 mL, 303 mmol) and ethanol (70 mL) was heated under reflux for 5 hr. After cooling, saturated aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=2/1-1/2) and recrystallized from hexane/ethyl acetate to give 5-[3-[3-(trifluoromethoxy)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazole-2-thiol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08492378B2 |
| Quelldatensatz | uspto-grants-2013_07 |
| ORD ID | ord-fba1d2cc8d5d4287b2273c83ed9c279d |
| Quellennotiz | uspto-grants-2013_07 |