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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855135Generated: November 2, 2026

3',4',5'-Trimethoxyacetophenone → 1-(3,4,5-trimethoxyphenyl)ethanol

https://huagongshe.com/reaction/1855135

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3',4',5'-TrimethoxyacetophenoneHCID 14345—
ReactantSodium t-butoxideHCID 23676156—
CatalystTris(triphenylphosphine)ruthenium(II) dichlorideHCID 84971—
SolventEthanolHCID 702—
Product1-(3,4,5-trimethoxyphenyl)ethanolHCID 254122—

Reaction Conditions

Temperature80 °C

Reaction Steps

Tris(triphenylphosphine)ruthenium(II) chloride (3.8 mg, 4 μmol, 1 mol %) and a chiral ligand (M=Ru, R=i-Pr, Ar=C6H5—, 2.6 μmol, 0.65 mol %) were dissolved in ethanol (3 mL) under nitrogen atmosphere, and then heated and stirred for 1 h at 80° C. After the mixture was cooled to room temperature, 3,4,5-trimethoxyacetophenone (0.4 mmol), ethanol (2 mL) and a solution of sodium t-butoxide in ethanol (0.4 mL, 0.2 M) were added thereto. Thereafter, the reaction system was placed in an autoclave, and stirred for 48 h under H2 (10 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-(3,4,5-trimethoxyphenyl)ethanol was obtained and the ee value (ee=97%) was measured by GC analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962852B2
Source datasetuspto-grants-2015_02
ORD IDord-1b6fced9cc98410d94c1a0142a2770f0
Source noteuspto-grants-2015_02