HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604594Generated: October 25, 2026
2'-Fluoro-4'-methoxyacetophenone → 2-(2-Fluoro-4-methoxyphenyl)-2-propanol
https://huagongshe.com/reaction/604594
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2'-Fluoro-4'-methoxyacetophenone | HCID 592821 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Fluoro-4-methoxyphenyl)-2-propanol | HCID 13493844 | — |
Reaction Steps
To a solution of 2′-fluoro-4′-methoxyacetophenone (4.45 g, 26.5 mmol) in dry THF (50 mL) at 0° C., a solution of 2.4 M methyl magnesium bromide (11.6 mL, 27.8 mmol) was added. The mixture was stirred at 0° C. and then room temperature for 4 h. The reaction was quenched with saturated NH4Cl solution. The organic was extracted with EtOAc (3×50 mL). The combined EtOAc layers were washed with brine and dried over Na2SO4. The resulting alcohol was obtained as an oil after flash chromatography using EtOAc:hexane=2:8 as the eluant.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910592B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-9a1bb05199f54be2b7b7cd02a6f352ce |
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| Source note | uspto-grants-2011_03 |
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