Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7472Erstellt: 23. Oktober 2026

Acetovanillone → 1-(4-Benzyloxy-3-methoxy-phenyl)-ethanone

https://huagongshe.com/de/reaction/7472

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetovanilloneHCID 2214—
EduktBenzyl BromideHCID 7498—
EduktPotassium CarbonateHCID 11430—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-(4-Benzyloxy-3-methoxy-phenyl)-ethanoneHCID 9921599%

Reaktionsschritte

The starting material, 4-benzyloxy-3-methoxyacetophenone, was obtained by heating a solution of 4-hydroxy-3-methoxyacetophenone (20 g, 0.12 mol), benzyl bromide (15.7 ml, 0.13 mol) and potassium carbonate (49.8 g, 0.36 mol), in DMF (400 ml) at 40° C. overnight. After cooling, the mixture was diluted with water, acidified to approximately pH3 and extracted with ethyl acetate. The organic layer was washed with brine, dried (MgSO4) and the solvent evaporated. The residue was purified by flash chromatography using petroleum ether/ethyl acetate (8/2 followed by 65/35) as eluent to give 4-benzyloxy-3-methoxyacetophenone (30.3 g, 99%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087602B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-5361ab59f70448ae8738fc7abac188e4
Quellennotizuspto-grants-2006_08