Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butyrophenone | HCID 10315 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Catalyst | Benzeneruthenium(II) Chloride Dimer | HCID 10962144 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 11819186 | HCID 11819186 | — |
Reaction Steps
Benzeneruthenium(II) chloride dimer (1.0 mg, 2 μmol, 0.5 mol %) and a chiral ligand (M=Ru, R=t-Bu, Ar=3,5-t-Bu2C6H3—, 2.6 μmol, 0.65 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, 1-phenylbutan-1-one (0.4 mmol), i-propanol (2 mL) and a solution of sodium hydroxide in i-propanol (0.4 mL, 0.4 M) were added thereto. Thereafter, the reaction system were placed in an autoclave, and stirred for 12 h under H2 (10 atm) at 40° C. The solvent was removed under reduced pressure, and the resultants were separated by column chromatography (silica gel column; eluent:ethyl acetate/petroleum ether=1/8). Accordingly, pure 1-phenylbutynol was obtained and the ee value (ee=99.2%) was measured by GC analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962852B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-dcdf5757de164be3b7b97df52b2bdb36 |
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| Source note | uspto-grants-2015_02 |
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