HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855117Generated: October 26, 2026
2-Methylacetophenone → 1-(2-Methylphenyl)ethanol
https://huagongshe.com/reaction/1855117
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methylacetophenone | HCID 11340 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Catalyst | Iron | HCID 23925 | — |
| Catalyst | Dichloro(p-cymene)ruthenium(II) dimer | HCID 10908223 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(2-Methylphenyl)ethanol | HCID 110953 | — |
Reaction Steps
Dichloro(p-cymene)ruthenium(II) dimer (1.2 mg, 2 μmol, 0.5 mol %) and a chiral ligand (M=Fe, R=i-Pr, Ar=C6H5—, 2.6 μmol, 0.65 mol %) were dissolved in toluene (3 mL) under nitrogen atmosphere, and then heated and stirred for 2 h at 120° C. After the mixture was cooled to room temperature, o-methylacetophenone (0.4 mmol), toluene (2 mL) and an aqueous solution of potassium hydroxide (0.4 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 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-(o-methylphenyl)ethanol was obtained and the ee value (ee=98%) 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-0a4663ac3c514b95b0c5d71703d12596 |
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| Source note | uspto-grants-2015_02 |
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