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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 920528Erstellt: 24. Oktober 2026

Trimethylsilyl triflate → 1-[4-(Benzyloxy)-3-methylphenyl]-2-bromoethanone

https://huagongshe.com/de/reaction/920528

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilyl triflateHCID 65367—
EduktN-bromobutanimideHCID 67184—
EduktDiisopropylethylamineHCID 81531—
EduktEthanone, 1-[3-methyl-4-(phenylmethoxy)phenyl]-HCID 12969325—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-[4-(Benzyloxy)-3-methylphenyl]-2-bromoethanoneHCID 1296932770,2%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 1-(4-benzyloxy-3-methyl-phenyl)-ethanone (12.89 g; 53.1 mmol) in CH2Cl2 was added, dropwise, at 0° C., DIPEA (10.9 mL; 63.7 mmol) and trimethylsilyl trifluoromethanesulfonate (11.1 mL; 61.1 mmol). The resulting mixture was stirred at 0° C. for 1 hour, and subsequently, NBS (10.87 g; 61.1 mmol) was added in one portion. The mixture was allowed to warm to RT stirred overnight. Then the mixture was concentrated in vacuo, the residue dissolved in EtOAc, washed with water twice, and brine, dried (MgSO4), filtered, and concentrated in vacuo to afford 1-(4-benzyloxy-3-methyl-phenyl)-2-bromo-ethanone (11.90 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09273017B2
Quelldatensatzuspto-grants-2016_03
ORD IDord-fe1b9589b55747c4ba87726a178f5938
Quellennotizuspto-grants-2016_03