HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855128Generated: November 2, 2026
Sodium Hydroxide → 1-(2,4-Difluorophenyl)ethanol
https://huagongshe.com/reaction/1855128
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,4-Difluoroacetophenone | HCID 67770 | — |
| Catalyst | Dichloro(p-cymene)ruthenium(II) dimer | HCID 10908223 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-(2,4-Difluorophenyl)ethanol | HCID 14653153 | — |
Reaction Steps
Dichloro(p-cymene)ruthenium(II) dimer (1.2 mg, 2 μmol, 0.5 mol %) and a chiral ligand (M=Ru, R=t-Bu, Ar=C6H5—, 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, 2,4-difluoroacetophenone (0.4 mmol), i-propanol (2 mL) and an aqueous solution of sodium hydroxide (1.0 mL, 0.2 M) were added thereto. Thereafter, the reaction system was placed in an autoclave, and stirred for 24 h under H2 (20 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-(2,4-difluorophenyl)ethanol was obtained and the ee value (ee=93%) 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-9443cb19849a4bedacad7a0e35dacb0e |
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| Source note | uspto-grants-2015_02 |
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