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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1855118Erstellt: 27. Oktober 2026

p-METHYLACETOPHENONE → p,alpha-DIMETHYLBENZYL ALCOHOL

https://huagongshe.com/reaction/1855118

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-METHYLACETOPHENONEHCID 8500—
EduktPotassium ethoxideHCID 23670592—
KatalysatorTris(triphenylphosphine)ruthenium(II) dichlorideHCID 84971—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelIsopropanolHCID 3776—
Produktp,alpha-DIMETHYLBENZYL ALCOHOLHCID 10817—

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

Tris(triphenylphosphine)ruthenium(II) chloride (3.8 mg, 4 μmol, 0.5 mol %) and a chiral ligand (M=Ru, R=t-Bu, Ar=C6H5—, 2.6 μmol, 0.33 mol %) were dissolved in ether (3 mL) under nitrogen atmosphere, and then heated and stirred for 1 h at 40° C. After the mixture was cooled to room temperature, p-methylacetophenone (0.8 mmol), ether (2 mL) and a solution of potassium ethoxide in i-propanol (0.4 mL, 0.2 M) were added thereto. Thereafter, the reaction system was placed in an autoclave, and stirred for 12 h under H2 (10 atm) at 25° 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-(p-methylphenyl)ethanol was obtained and the ee value (ee=99.3%) was measured by GC analysis.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08962852B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-ead8dc1ea0614d72b4c68ceebf430b92
Quellennotizuspto-grants-2015_02