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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370827Generated: October 27, 2026

Potassium Carbonate → 4-[4-(Allyloxy)phenoxy]benzaldehyde

https://huagongshe.com/reaction/1370827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-FluorobenzaldehydeHCID 68023—
Reactant4-(Allyloxy)phenolHCID 1713883—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product4-[4-(Allyloxy)phenoxy]benzaldehydeHCID 1851218281%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-Fluorobenzaldehyde (3.8 mL, 35.1 mmoles) was added to a solution of the product from Example 60A (4.39 g, 29.3 mmoles) and K2CO3 (8.90 g, 64.4 mmoles) in DMF (29.3 mL). The resulting mixture was heated to 100° C. for 2.5 days and then cooled to room temperature. The crude products were diluted with diethyl ether, extracted with sat. NH4Cl, extracted with H2O (2×), washed with brine, dried (Na2SO4), and concentrated under reduced pressure. The residue was purified by flash chromatography on a prepacked Biotage column (hexane→9:1 hexane:ethyl acetate) on silica gel to provide the title compound (3.50 g, 81%) as a clear colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583180B2
Source datasetuspto-grants-2003_06
ORD IDord-6ec84693bfce4f2ba7bac6e36062ed87
Source noteuspto-grants-2003_06