HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Methanol → 4-(5-Methoxy-tetrahydro-furan-3-yl)-benzoic Acid Ethyl Ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Benzocaine | HCID 2337 | — |
| Edukt | 2,5-Dihydrofuran | HCID 15570 | — |
| Edukt | Tetrafluoroboric acid | HCID 28118 | — |
| Edukt | Sodium Nitrite | HCID 23668193 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-(5-Methoxy-tetrahydro-furan-3-yl)-benzoic Acid Ethyl Ester | HCID 69365300 | — |
Reaktionsschritte
A solution of sodium nitrite (1.67 g, 24.2 mmol) in water (14 mL) is added dropwise to an ice cold mixture of ethyl 4-aminobenzoate (4.0 g, 24.2 mmol) and tetrafluoroboric acid (7.8 mL, 48%, 59.78 mmol) and stirred for 30 min. Methanol (28.5 mL), 2,5-dihydrofuran (3.66 mL, 48.4 mmol) and palladium(II) acetate (70 mg, 0.31 mmol) are added and the mixture refluxed for 30 min. The mixture is filtered through Celite® pad and the filtrate diluted with dichloromethane (100 mL). The organic layer is separated and concentrated in vacuo. The residue is chromatographed on SiO2 (10% ethyl acetate/hexanes) to yield the title compound, 2.45 g (42%), as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07087626B2 |
| Quelldatensatz | uspto-grants-2006_08 |
| ORD ID | ord-e7582e27591542cc9b1ae12d23cd68f8 |
| Quellennotiz | uspto-grants-2006_08 |