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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1855133Erstellt: 26. Oktober 2026

2-Acetylnaphthalene → alpha-Methylnaphthalene-2-methanol

https://huagongshe.com/reaction/1855133

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AcetylnaphthaleneHCID 7122—
EduktPotassium HydroxideHCID 14797—
KatalysatorTris(triphenylphosphine)ruthenium(II) dichlorideHCID 84971—
LösungsmittelDichloromethaneHCID 6344—
Produktalpha-Methylnaphthalene-2-methanolHCID 98243—

Reaktionsbedingungen

Temperatur40 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08962852B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-6014b161c2634b96a5b4faead481fbf1
Quellennotizuspto-grants-2015_02