HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855133Generated: October 26, 2026
2-Acetylnaphthalene → alpha-Methylnaphthalene-2-methanol
https://huagongshe.com/reaction/1855133
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Acetylnaphthalene | HCID 7122 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Catalyst | Tris(triphenylphosphine)ruthenium(II) dichloride | HCID 84971 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | alpha-Methylnaphthalene-2-methanol | HCID 98243 | — |
Reaction Steps
Tris(triphenylphosphine)ruthenium(II) chloride (3.8 mg, 4 μmol, 1 mol %) and a chiral ligand (M=Ru, R=t-Bu, Ar=3,5-t-Bu2C6H3—, 2.6 μmol, 0.65 mol %) were dissolved in dichloromethane (3 mL) under nitrogen atmosphere, and then heated and stirred for 0.5 h at 40° C. After the mixture was cooled to room temperature, 2-acetonaphthone (0.4 mmol), dichloromethane (2 mL) and an aqueous solution of potassium hydroxide (0.2 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 50° 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-(2-naphthyl)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-6014b161c2634b96a5b4faead481fbf1 |
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| Source note | uspto-grants-2015_02 |
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