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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 860524Erstellt: 26. Oktober 2026

Potassium Carbonate → 4-[3-(1-Adamantyl)-4,5-methylenedioxyphenyl]-benzaldehyde

https://huagongshe.com/reaction/860524

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt4-Formylphenylboronic AcidHCID 591073—
Edukt3-(1-Adamantyl)-4,5-methylenedioxybromobenzeneHCID 19429702—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelWaterHCID 962—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-[3-(1-Adamantyl)-4,5-methylenedioxyphenyl]-benzaldehydeHCID 1015544385%

Reaktionsschritte

A mixture of 3-(1-adamantyl)-4,5-methylenedioxy-1-bromobenzene (2.00 g, 5.97 mmol), 4-formylphenylboronic acid (1.07 g, 7.16 mmol) and potassium carbonate (1.86 g, 13.42 mmol) in 1,2-dimethoxyethane (50 mL) and water (2.5 mL) was degassed with argon for 30 minutes. Tetrakis(triphenylphosphine)palladium(0) (0.34 g, 0.298 mmol) was added and the mixture heated at reflux under argon overnight. The solution was cooled to room temperature, diluted with ethyl acetate (200 mL) and washed successively with water (100 mL) and brine (100 mL), dried over anhydrous magnesium sulfate, filtered and evaporated. The residue was purified on silica gel (eluent: hexane:ethyl acetate, 95:5) to give 1.82 g of 4-[3-(1-Adamantyl)-4,5-methylenedioxy phenyl]-benzaldehyde (85%). 1H NMR (500 MHz; CDCl3): δ 1.79 (s, 6H); 2.08 (s, 9H); 6.01 (s, 2H); 7.00 (d, J=2.0 Hz, 1H); 7.04 (d, J=2.0 Hz, 1H); 7.68 (d, J=8.1 Hz, 2H); 7.91 (d, J=8.1 Hz, 2H); 10.03 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07153875B2
Quelldatensatzuspto-grants-2006_12
ORD IDord-2c2ad17e4fa14963a579d3c92f029f61
Quellennotizuspto-grants-2006_12