HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Dichloromethane → (4-Phenylfuran-3-yl)methanol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | Ethyl-4-phenyl-3-furoate | HCID 15037153 | — |
| Edukt | Diisobutylaluminumhydride | HCID 21225700 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | (4-Phenylfuran-3-yl)methanol | HCID 15037154 | 72,9% |
Reaktionsschritte
Prepare a solution of 4-phenylfuran-3-carboxylic acid ethyl ester (3.9 g, 18.1 mmol) in toluene (20 mL) under nitrogen at −78° C. Add a 1.0 M solution of Diisobutyl aluminium hydride in methylene chloride (35 mL, 35.0 mmol). Stir the reaction mixture for 1 hour, quench with water, and pour into 10% Rochelle's salt (200 mL). Extract the aqueous phase with ethyl acetate (2×200 mL). Wash the organic phase with brine (100 mL), dry (Na2SO4), filter, and concentrate. Flash chromatography on silica gel eluting with 4:1 Hex/ethyl acetate to afford 2.3 g of (4-phenylfuran-3-yl)methanol. 1H NMR (CDCl3) δ 7.51-7.58 (m, 4H), 7.30-7.45 (m, 3H), 4.67 (d, J=5 Hz, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07265246B2 |
| Quelldatensatz | uspto-grants-2007_09 |
| ORD ID | ord-6241da7920634465ac54be5c5f0f9452 |
| Quellennotiz | uspto-grants-2007_09 |