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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3682Generated: October 25, 2026

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

https://huagongshe.com/reaction/3682

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 (5 g), 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 for reacting them together. To the reaction solution was added ethyl acetate (300 ml), and the resulting solution was washed in dilute hydrochloric acid, in water, and in a 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 numberUS05734067
Source datasetuspto-grants-1998_03
ORD IDord-b4abd6c40e154847ac62183456b57efd
Source noteuspto-grants-1998_03