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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2167835Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2167835

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktPotassium CarbonateHCID 11430—
Edukt4'-Hydroxy-3'-methylacetophenoneHCID 70135—
LösungsmittelAcetoneHCID 180—
ProduktEthanone, 1-[3-methyl-4-(phenylmethoxy)phenyl]-HCID 1296932599,1%

Reaktionsschritte

A mixture of 4′-hydroxy-3′-methylacetophenone (10.00 g; 66.6 mmol) and K2CO3 (13.80 g; 99.9 mmol) in acetone (100 mL) was stirred, at RT for 40 minutes. Subsequently, benzyl bromide (7.9 mL; 66.6 mmol) was added and the resulting mixture was heated under reflux for 2.5 h. After cooling to RT the mixture was concentrated in vacuo. The residue was dissolved in EtOAc, washed with 5% aqueous ammonia, water, and brine, dried (MgSO4), filtered and concentrated in vacuo to afford 1-(4-benzyloxy-3-methylphenyl)-ethanone (15.86 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09045441B2
Quelldatensatzuspto-grants-2015_06
ORD IDord-eee07cea7e334acc82d58ad89ec6569c
Quellennotizuspto-grants-2015_06