Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Acetylbiphenyl | HCID 7113 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-(4-Biphenylyl)ethanol | HCID 96176 | — |
Reaction Steps
Tris(triphenylphosphine)ruthenium (II) chloride (1.9 mg, 2 μmol, 0.5 mol %) and a chiral ligand (M=Ru, R=i-Pr, Ar=C6H5—, 1.3 μmol, 0.33 mol %) were dissolved in i-propanol (3 mL) under nitrogen atmosphere, and then heated and stirred for 1 h at 85° C. After the mixture was cooled to room temperature, p-phenyl-acetophenone (0.8 mmol), i-propanol (2 mL) and a solution of potassium carbonate in i-propanol (0.8 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 −20° 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-phenylphenyl)ethanol was obtained and the ee value (ee=99.2%) was measured by GC analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08962852B2 |
|---|
| Source dataset | uspto-grants-2015_02 |
|---|
| ORD ID | ord-501781a76bdd4aae95ab7e2e8566cbd4 |
|---|
| Source note | uspto-grants-2015_02 |
|---|