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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Fluoro-3-methoxyphenyl)-2-phenylethanolHCID 59458896—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
Product1-(4-Fluoro-3-methoxyphenyl)-2-phenylethanoneHCID 59458409151.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304403B2
Source datasetuspto-grants-2012_11
ORD IDord-5ebb5e05322e46a9a598a67faa0717ad
Source noteuspto-grants-2012_11