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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 460020Erstellt: 24. Oktober 2026

Benzyl Bromide → Ethanone, 1-[3-methyl-4-(phenylmethoxy)phenyl]-

https://huagongshe.com/de/reaction/460020

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktPotassium CarbonateHCID 11430—
Edukt4'-Hydroxy-3'-methylacetophenoneHCID 70135—
LösungsmittelAcetonitrileHCID 6342—
ProduktEthanone, 1-[3-methyl-4-(phenylmethoxy)phenyl]-HCID 12969325—

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

A mixture of 4-hydroxy-3-methylacetophenone (5.0 g) in dry acetonitrile (50 ml) was treated with potassium carbonate (5.06 g) and benzyl bromide (3.96 ml) and the reaction mixture heated at 40° C. After 3 hours the reaction was allowed to cool and was concentrated. The residue was partitioned between water and ethyl acetate; the aqueous layer separated and extracted twice more with ethyl acetate. The organic solutions were combined and were dried with brine and over magnesium sulfate and concentrated to give the title compound as a colourless oil

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07196107B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-da235d1cfd0447f28bdf62d1f7e867b5
Quellennotizuspto-grants-2007_03