HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
{2-Ethyl-5-[4-(trifluoromethyl)phenyl]-3-furyl}methanol → 2-Ethyl-5-[4-(trifluoromethyl)phenyl]-3-furaldehyde
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | {2-Ethyl-5-[4-(trifluoromethyl)phenyl]-3-furyl}methanol | HCID 23074480 | — |
| Katalysator | HCID 178418406 | HCID 178418406 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-Ethyl-5-[4-(trifluoromethyl)phenyl]-3-furaldehyde | HCID 23074355 | 24,6% |
Reaktionsbedingungen
| Temperatur | 40 °C |
|---|
Reaktionsschritte
A suspension of {2-ethyl-5-[4-(trifluoromethyl)phenyl]-3-furyl}methanol (2.7 g) and manganese dioxide (6.8 g) in diethyl ether (20 mL) and tetrahydrofuran (20 mL) was stirred overnight at 40° C. Manganese dioxide was filtered off, and the filtrate was evaporated under reduced pressure. The residue was purified by silica gel chromatography (5% ethyl acetate/hexane to 20% ethyl acetate/hexane), and crystallized from ethyl acetate/hexane to give the title compound (0.66 g, 24%) as a yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08309580B2 |
| Quelldatensatz | uspto-grants-2012_11 |
| ORD ID | ord-702d166f9b8142d3b86b750a9e79e101 |
| Quellennotiz | uspto-grants-2012_11 |