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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 384143Erstellt: 24. Oktober 2026

Hydrochloric Acid → o-Phenoxybenzaldehyde

https://huagongshe.com/de/reaction/384143

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPhenolHCID 996—
EduktPotassium CarbonateHCID 11430—
Edukto-FluorobenzaldehydeHCID 67970—
LösungsmittelDimethylformamideHCID 6228—
Produkto-PhenoxybenzaldehydeHCID 88060—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 2-fluorobenzaldehyde (0.5 ml) in dimethylformamide (5 ml), 676 mg of phenol and 993 mg of potassium carbonate were added, and the reaction solution was stirred overnight at 100° C. The reaction solution was cooled, then 1N hydrochloric acid was added, and the mixture was extracted with ethyl acetate. The combined organic layers were washed with a saturated saline solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue obtained was purified by silica gel column chromatography (eluent: hexane/ethyl acetate (98:2-50/50)) to afford the title compound as a pale yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367708B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-3ed9157d285e4c319744798e9acf5d0a
Quellennotizuspto-grants-2013_02