HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874189Generated: October 27, 2026
1-(4-Fluoro-3-methoxyphenyl)-2-phenylethanol → 1-(4-Fluoro-3-methoxyphenyl)-2-phenylethanone
https://huagongshe.com/reaction/1874189
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(4-Fluoro-3-methoxyphenyl)-2-phenylethanol | HCID 59458896 | — |
| Reactant | Jones' reagent | HCID 131709961 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-(4-Fluoro-3-methoxyphenyl)-2-phenylethanone | HCID 59458409 | 151.3% |
Reaction Steps
To a solution of 1-(4-fluoro-3-methoxyphenyl)-2-phenylethanol (23.7 g, 40.6 mmol) in acetone (240 mL) was added Jones reagent (64 mL) at rt. The reaction mixture was stirred overnight, quenched by the addition of isopropanol and diluted with EtOAc. The organic portion was washed with 1 N HCl (2×), dried over Na2SO4, filtered and concentrated under reduced pressure to yield the 1-(4-fluoro-3-methoxyphenyl)-2-phenylethanone (15 g, 66% yield). LCMS: RT=3.250 min [M+H] 245.1 (Phenomenex Luna C18 column, 4.6×50 mm eluting with 10-90% MeOH/H2O over 4 minutes containing 0.1% NH4OAc; 4 mL/min, monitoring at 220 nm); 1H NMR (500 MHz, CDCl3) δ ppm 7.62 (dd, J=8, 1 Hz, 1H), 7.60-7.55 (m, 1 H), 7.35-7.29 (m, 2H), 7.26-7.23 (m, 3H), 7.10 (dd, J=10, 8 Hz, 1H), 4.24 (s, 2H), 3.89 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304403B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-5ebb5e05322e46a9a598a67faa0717ad |
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| Source note | uspto-grants-2012_11 |
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