HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446584Generated: October 26, 2026
1-(4-Fluoro-3-methoxyphenyl)ethanone → (αR)-4-Fluoro-3-methoxy-α-methylbenzenemethanol
https://huagongshe.com/reaction/1446584
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(4-Fluoro-3-methoxyphenyl)ethanone | HCID 2774532 | — |
| Reactant | HCID 13515831 | HCID 13515831 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (αR)-4-Fluoro-3-methoxy-α-methylbenzenemethanol | HCID 26597270 | 90.7% |
Reaction Steps
A solution of 4-fluoro-3-methoxyacetophenone (1 g) in THF (10 mL) was added dropwise to a solution of (+)-DIPCl™ (2.29 g) in THF (30 mL) in a nitrogen atmosphere at −20° C., and the reaction solution was stirred at −20° C. for 5 hours. The reaction solution was heated to room temperature, and the solvent was evaporated under reduced pressure. The residue was diluted with an ether, diethanolamine (1.25 mL) was added to the diluent, and the reaction solution was stirred at room temperature overnight. The reaction solution was filtered on a celite, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent:heptane-ethyl acetate system) to obtain 918 mg of the title compound. The physical properties of the compound are as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07667041B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-182d884889e94a60a98c5de05fb9ba4b |
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| Source note | uspto-grants-2010_02 |
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