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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 3682Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/3682

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-PentanolHCID 6276—
EduktPotassium CarbonateHCID 11430—
Edukt2'-BromoacetophenoneHCID 75060—
Edukt2,3-DimethoxyphenolHCID 78828—
KatalysatorCupric acetateHCID 8895—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(2,3-Dimethoxyphenoxy)acetophenoneHCID 1837995587%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05734067
Quelldatensatzuspto-grants-1998_03
ORD IDord-b4abd6c40e154847ac62183456b57efd
Quellennotizuspto-grants-1998_03