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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360354Generated: November 3, 2026

3-Methoxyphenol → 4-(3-Methoxyphenoxy)benzaldehyde

https://huagongshe.com/reaction/2360354

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxyphenolHCID 9007—
ReactantCesium carbonateHCID 10796—
Reactant4-FluorobenzaldehydeHCID 68023—
SolventDimethylformamideHCID 6228—
Product4-(3-Methoxyphenoxy)benzaldehydeHCID 16244084100%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of p-fluorobenzaldehyde (1.6 mmol, 0.2 g) in dimethylformamide (8 mLs) was added 3-methoxyphenol (3.52 mmol, 0.437 g) and cesium carbonate (3.52 mmol, 1.15 g). The reaction was heated to 90° C. for 3 hours at which time it was cooled to room temperature and filtered through a fritted funnel. The reaction mixture was diluted with 125 mL of ethyl acetate and extracted with eight 15 mL portions of water and one 10 mL portion of brine. The organic layer was dried with magnesium sulfate and evaporated to dryness. The crude oil was purified by flash chromatography to recover 0.365 g (1.6 mmol) of the title product. 1H NMR (300 MHz, CDCl3) δ 9.92 (s, 1H), 7.84 (d, J=8.7, 2H), 7.29 (dd, J=5.7, 13.9, 1H), 7.07 (d, J=8.7, 2H), 6.76 (d, J=8.3, 1H), 6.72-6.57 (m, 2H), 3.80 (s, 3H). 13C NMR (75 MHz, CDCl3) δ 190.99, 163.25, 161.38, 156.42, 132.15, 130.76, 117.91, 112.63, 110.81, 106.59, 55.66.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686046B2
Source datasetuspto-grants-2014_04
ORD IDord-00bb84e003e449ba937238341536f3b2
Source noteuspto-grants-2014_04