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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712732Generated: October 27, 2026

1-(4-Fluoro-3-methoxyphenyl)-2-phenylethanol → 1-(4-Fluoro-3-methoxyphenyl)-2-phenylethanone

https://huagongshe.com/reaction/1712732

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, 1H), 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 numberUS07790770B2
Source datasetuspto-grants-2010_09
ORD IDord-f88afba199ae446ba06e459aa0197456
Source noteuspto-grants-2010_09