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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11201Erstellt: 23. Oktober 2026

Benzyl Bromide → 1-Bromo-4-phenylmethoxybenzene

https://huagongshe.com/de/reaction/11201

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
Edukt4-BromophenolHCID 7808—
EduktPotassium CarbonateHCID 11430—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-Bromo-4-phenylmethoxybenzeneHCID 138835—

Reaktionsschritte

4-Bromophenol (2 g, 0.0116 mol) in acetone (40 ml) was treated with potassium carbonate (1.91 g, 1.2 equivalents) and benzyl bromide (1.44 ml, 1.05 equivalents). The reaction was refluxed under nitrogen. After 5–6 hours of reflux, the reaction was cooled to room temperature and diluted with an equal volume of ethyl acetate. This was diluted further with water and the organic layer was separated, dried over magnesium sulfate and evaporated to dryness to afford a white fluffy powder. Yield=2.36 g (73%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07097995B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-9c38a67482a74a60b22a9dd04f69b8a7
Quellennotizuspto-grants-2006_08