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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 412166Erstellt: 24. Oktober 2026

Allyl bromide → 2-Benzyloxy-5-[(2-propenyl)oxy]benzaldehyde

https://huagongshe.com/de/reaction/412166

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl bromideHCID 7841—
EduktEthyl AcetateHCID 8857—
EduktPotassium CarbonateHCID 11430—
Edukt2-(Benzyloxy)-5-hydroxybenzaldehydeHCID 18536192—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-Benzyloxy-5-[(2-propenyl)oxy]benzaldehydeHCID 18536183—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a solution of the product from Step A (75.4 mmol) in 100 mL of DMF was added potassium carbonate (20.8 g, 150.7 mmol), followed by allyl bromide (11.7 mL, 135 mmol). The reaction was warmed to 60° C. and stirred for one hour. The solution was poured into EtOAc and washed with water, saturated NaHCO3 solution and brine, dried (Na2SO4), filtered, and concentrated in vacuo. The resulting product was purified by silica gel chromatography (20-30% EtOAc/hexane) to provide the titled product, along with unreacted starting material (4.39 g, 26%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06562823B1
Quelldatensatzuspto-grants-2003_05
ORD IDord-1b40a4cf657d453cb3e06a20ba23ab57
Quellennotizuspto-grants-2003_05