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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 390208Erstellt: 25. Oktober 2026

Phenol → 2-Nitro-5-phenoxybenzaldehyde

https://huagongshe.com/reaction/390208

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenolHCID 996—
EduktPotassium CarbonateHCID 11430—
Edukt5-Fluoro-2-nitrobenzaldehydeHCID 587090—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelHexaneHCID 8058—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-Nitro-5-phenoxybenzaldehydeHCID 44203082—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

A mixture of 5-fluoro-2-nitrobenzaldehyde (15.00 g, 0.089 mol), phenol (9.12 g, 0.098 mol), and K2CO3 (13.5 g, 0.089 mol) in 200 mL of DMF was heated at 120° C. for 50 min. The reaction mixture was cooled and concentrated in vacuo. To the residue was added EtOAc (500 mL) and H2O (500 mL). The layers were separated, and the EtOAc extract was concentrated. The residue was purified on silica gel using 20% EtOAc-hexane as eluent. The product containing fractions were combined and concentrated to yield a yellow oil which solidified on standing. This material was dissolved in a minimal quantity of EtOAc and hexane, and the resulting solution was cooled in a dry ice acetone bath. Filtration yielded 2-nitro-5-phenoxy-benzaldehyde as a light yellow solid. The filtrate was concentrated in vacuo to yield additional 2-nitro-5-phenoxy-benzaldehyde.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08383637B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-0a2736780b214673a916a05ce48aa6d6
Quellennotizuspto-grants-2013_02