Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | (4-Phenylfuran-3-yl)methanol | HCID 15037154 | — |
| Katalysator | HCID 178419074 | HCID 178419074 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-Phenyl-3-furaldehyde | HCID 15037148 | 59,8% |
Reaktionsschritte
Prepare a solution of (4-phenylfuran-3-yl)methanol (2.3 g, 13.2 mmol) in methylene chloride (20 mL). Add N-methylmorpoline N-oxide (2.2 g, 18.5 mmol) and powdered 4 Å molecular sieves. Cool the mixture to 0° C. and add tetra-n-propyl ammonium perruthenate. Warm the mixture to room temperature and stir for an additional 3 hours. Filter the reaction mixture through Celite® and concentrate the filtrate. Perform flash chromatography on silica gel eluting with 10% diethyl ether/hexane to afford 1.36 g of 4-phenyl-3-formylfuran. 1H NMR (CDCl3) δ 10.01 (s, 1H), 8.15 (s, 1H), 7.60 (s, 1H), 7.35-7.54 (m, 5H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07265246B2 |
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| Quelldatensatz | uspto-grants-2007_09 |
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| ORD ID | ord-d01dd0173fa64666a2494a297d85a9a0 |
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| Quellennotiz | uspto-grants-2007_09 |
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