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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 547609Erstellt: 26. Oktober 2026

4-Hydroxybenzyl Alcohol → {4-[(3,4-Dinitrophenyl)oxy]phenyl}methanol

https://huagongshe.com/reaction/547609

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Hydroxybenzyl AlcoholHCID 125—
EduktCesium carbonateHCID 10796—
EduktPotassium CarbonateHCID 11430—
Edukt3,4-DinitrofluorobenzeneHCID 298675—
LösungsmittelDimethylformamideHCID 6228—
Produkt{4-[(3,4-Dinitrophenyl)oxy]phenyl}methanolHCID 5758591045,2%

Reaktionsschritte

4-fluoro-1,2-dinitrobenzene (20.0 g, 107.5 mmol), 4-(hydroxymethyl)phenol (14.7 g, 118.2 mmol) and potassium carbonate (17.8 g, 129.0 mmol) were stirred in 250 ml of dimethylformamide at room temperature for approximately 17 hours. The reaction was heated at 35 degree Centigrade for 1.5 hours. Cesium carbonate (2 g, 6.14 mmol) was added and the reaction was heated at 45 deg. C. for approximately 22 hours. The solids were filtered away and washed with ethyl acetate. The filtrate was diluted with water and extracted 4 times with ethyl acetate. The ethyl acetate layers were washed with a water/brine mixture 5 times. The aqueous wash layers were back extracted with ethyl acetate twice. The organic layers were combined, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (0 to 100% ethyl acetate in hexane) to give 14.1 g of {4-[(3,4-dinitrophenyl)oxy]phenyl}methanol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07939528B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-1e841c2472d34406894f9a6e49077704
Quellennotizuspto-grants-2011_05