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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 653656Erstellt: 24. Oktober 2026

Potassium Carbonate → 3-(Bicyclo[2.2.1]hept-2-yloxy)-4-methoxybenzaldehyde

https://huagongshe.com/de/reaction/653656

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktIsovanillinHCID 12127—
Edukt2-Norbornyl bromideHCID 98232—
LösungsmittelWaterHCID 962—
Produkt3-(Bicyclo[2.2.1]hept-2-yloxy)-4-methoxybenzaldehydeHCID 1401015287,2%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Isovanillin (50 g, 0.328 mol) is placed in a 1 liter round bottom flask which is equipped with a stir bar and reflux condensor and is charged with 500 ml of dimethylformamimde. Potassium carbonate (45.3 g, 0.328 mol) is added to the reaction mixture which is heated to 80° C. At this temperature exo-2-bromonorbornane (12.57 g, 0.072 mol, 0.219 equivalents) is added and the reaction mixture is heated to 120° C. for 48 hours. The reaction is then cooled to room temperature and poured into 300 ml of water. The aqueous layer is extracted with ethyl ether (3×100 ml). The ethereal layer is washed with 1N sodium hydroxide solution (4×100 ml), water (3×100 ml) and saturated sodium chloride solution (3×100 ml). The organic layer is dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to yield 15.47 g of a green/brown oil. The crude product is purified by flash chromatography using a gradient eluent system of ethyl acetate/hexane [10% ethyl acetate/hexane→20% ethyl acetate/hexane] to yield 7.76 g (14.4%) of the aldehyde as a white solid. MP: 75.5° C.-79.5° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05128358
Quelldatensatzuspto-grants-1992_07
ORD IDord-45335419ac44489ea57b154ebaeb6879
Quellennotizuspto-grants-1992_07