Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Acetylnaphthalene | HCID 13663 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Katalysator | Iron | HCID 23925 | — |
| Katalysator | Tris(triphenylphosphine)ruthenium(II) dichloride | HCID 84971 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 1-(1-Naphthyl)ethanol | HCID 98030 | — |
Reaktionsschritte
Tris(triphenylphosphine)ruthenium(II) chloride (3.8 mg, 4 μmol, 1 mol %) and a chiral ligand (M=Fe, R=Me, Ar=C6H5—, 2.6 μmol, 0.65 mol %) were dissolved in 1,4-dioxane (3 mL) under nitrogen atmosphere, and then heated and stirred for 2 h at 105° C. After the mixture was cooled to room temperature, 1-acetonaphthone (0.4 mmol), 1,4-dioxane (2 mL) and a solution of potassium t-butoxide in 1,4-dioxane (0.4 mL, 0.4 M) were added thereto. Thereafter, the reaction system was placed in an autoclave, and stirred for 24 h under H2 (40 atm) at 0° C. The solvent was removed under reduced pressure, and the resultants were separated by column chromatography (silica gel column; eluent: ethyl acetate/petroleum ether=1/5). Accordingly, pure 1-(1-naphthyl)ethanol was obtained and the ee value (ee=98%) was measured by GC analysis.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08962852B2 |
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| Quelldatensatz | uspto-grants-2015_02 |
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| ORD ID | ord-d8bd60830b21433195e3d279c575b9b1 |
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| Quellennotiz | uspto-grants-2015_02 |
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