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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567868Generated: October 26, 2026

1-Pentanol → 2-(2,3-Dimethoxyphenoxy)acetophenone

https://huagongshe.com/reaction/567868

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PentanolHCID 6276—
ReactantPotassium CarbonateHCID 11430—
Reactant2'-BromoacetophenoneHCID 75060—
Reactant2,3-DimethoxyphenolHCID 78828—
CatalystCupric acetateHCID 8895—
SolventEthyl AcetateHCID 8857—
Product2-(2,3-Dimethoxyphenoxy)acetophenoneHCID 1837995587%

Reaction Conditions

Temperature150 °C

Reaction Steps

Amyl alcohol (44 ml) was added to 2,3-dimethoxyphenol (5g), 2′-bromoacetophenone (7 g), potassium carbonate (6.7 g) and copper acetate (1.1 g), followed by heating and stirring at 150° C. for 8 hours. To the reaction solution was added ethyl acetate (300 ml), and the resulting solution was washed in dilute hydrochloric acid, in water, and in an aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvents therein were distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: hexane:ethyl acetate=8:1), to recover 2-(2,3-dimethoxyphenoxy)acetophenone (7.6 g; yield of 87%). By 1H-NMR (90 MHz, CDCl3), the compound has the peaks shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180659B2
Source datasetuspto-grants-2001_01
ORD IDord-1f70a90682d94de8b043f640ec629822
Source noteuspto-grants-2001_01