HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1855133Erstellt: 26. Oktober 2026
2-Acetylnaphthalene → alpha-Methylnaphthalene-2-methanol
https://huagongshe.com/reaction/1855133
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Acetylnaphthalene | HCID 7122 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Katalysator | Tris(triphenylphosphine)ruthenium(II) dichloride | HCID 84971 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | alpha-Methylnaphthalene-2-methanol | HCID 98243 | — |
Reaktionsschritte
Tris(triphenylphosphine)ruthenium(II) chloride (3.8 mg, 4 μmol, 1 mol %) and a chiral ligand (M=Ru, R=t-Bu, Ar=3,5-t-Bu2C6H3—, 2.6 μmol, 0.65 mol %) were dissolved in dichloromethane (3 mL) under nitrogen atmosphere, and then heated and stirred for 0.5 h at 40° C. After the mixture was cooled to room temperature, 2-acetonaphthone (0.4 mmol), dichloromethane (2 mL) and an aqueous solution of potassium hydroxide (0.2 mL, 0.2 M) were added thereto. Thereafter, the reaction system was placed in an autoclave, and stirred for 24 h under H2 (10 atm) at 50° 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-(2-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-6014b161c2634b96a5b4faead481fbf1 |
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| Quellennotiz | uspto-grants-2015_02 |
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