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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 132589Erstellt: 25. Oktober 2026

2-Nitrophenol → 1-(Benzhydryloxy)-2-nitrobenzene

https://huagongshe.com/reaction/132589

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-NitrophenolHCID 6947—
EduktPotassium CarbonateHCID 11430—
EduktBromodiphenylmethaneHCID 236603—
EduktPotassiumHCID 5462222—
LösungsmittelAcetoneHCID 180—
Produkt1-(Benzhydryloxy)-2-nitrobenzeneHCID 743412239,5%

Reaktionsschritte

A mixture of o-nitrophenol (2.08 g, 15.0 mmol), 1-[bromo(phenyl)methyl]benzene (3.70 g, 15.0 mmol) and potassium carbonated (K2CO3) (4.14 g, 30.0 mmol) in acetone (60 mL) was kept at reflux temperature for 5 h. The reaction mixture was cooled to room temperature, concentrated in vacuo. The residue was partitioned between dichloromethane (CH2Cl2) and water (H2O), organic layer dried over sodium sulphate (Na2SO4), filtered, concentrated. The residue was purified by silica gel flash chromatography to give subtitled compound (1.81 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07388020B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-079031298525448db5b6e52e03b4a7e2
Quellennotizuspto-grants-2008_06