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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19987Erstellt: 23. Oktober 2026

Benzyl Bromide → 2-(Benzyloxy)-1-methoxy-4-nitrobenzene

https://huagongshe.com/de/reaction/19987

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktPotassium CarbonateHCID 11430—
Edukt2-Methoxy-5-nitrophenolHCID 69471—
LösungsmittelAcetoneHCID 180—
Produkt2-(Benzyloxy)-1-methoxy-4-nitrobenzeneHCID 531403696,5%

Reaktionsschritte

Potassium carbonate (1.65 gm; 12 mmol) was added to a solution of 2-methoxy-5-nitro phenol (1.69 g; 10 mmol) and benzyl bromide (1.71 gm; 10 mmol) in acetone (60 ml). The reaction mixture was refluxed for 12 hours. The solvent was removed under reduced pressure and the residue was partitioned between ethyl acetate (150 ml) and water (50 ml). The ethyl acetate layer was separated, washed with water (2×50 ml), dried over anhydrous magnesium sulfate. Removal of the solvent under reduced pressure provided 2.5 g of 1-Benzyloxy-2-methoxy-5-nitrobenzene (Yield=96.5%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745490B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-dfb5a266abc740b7aeafad57481660b5
Quellennotizuspto-grants-2010_06