Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1855132Erstellt: 25. Oktober 2026

1-Acetylnaphthalene → 1-(1-Naphthyl)ethanol

https://huagongshe.com/reaction/1855132

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-AcetylnaphthaleneHCID 13663—
EduktPotassium tert-butoxideHCID 23665647—
KatalysatorIronHCID 23925—
KatalysatorTris(triphenylphosphine)ruthenium(II) dichlorideHCID 84971—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt1-(1-Naphthyl)ethanolHCID 98030—

Reaktionsbedingungen

Temperatur105 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08962852B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-d8bd60830b21433195e3d279c575b9b1
Quellennotizuspto-grants-2015_02