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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1716206Erstellt: 25. Oktober 2026

Triethylamine → 4-Formylcinnamic acid tert-butyl ester

https://huagongshe.com/reaction/1716206

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukttert-Butyl acrylateHCID 15458—
Edukt4-BromobenzaldehydeHCID 70741—
EduktSodium BicarbonateHCID 516892—
KatalysatorTriphenylphosphineHCID 11776—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-Formylcinnamic acid tert-butyl esterHCID 5414760470%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A solution of 4-bromo benzaldehyde (2 g, 10.8 mmol) in DMF (50 ml) and triethylamine (3.4 ml, 27 mmol) was degassed flushing N2 for 30 min. PPh3 (141 mg, 0.54 mmol), Pd(OAc)2 (48.4 mg, 0.21 mmol), NaHCO3 (1.84 g, 21.6 mmol) and tert-butyl acrylate (1.58 ml, 10.8 mmol) were added and the resulting mixture was heated to reflux for 3 h. Additional Pd(OAc)2 (24 mg) was added and the mixture was heated to 100° C. for 1 h. The solution was diluted with H2O and extracted with Et2O. The organic layer was dried over Na2SO4 and the solvent was evaporated under vacuo to give the crude product that was triturated in isopropyl ether to give 1.6 g of 3-(4-formyl-phenyl)-acrylic acid tert-butyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07803800B2
Quelldatensatzuspto-grants-2010_09
ORD IDord-3d8f8591fd074ba7868e16a6c640501a
Quellennotizuspto-grants-2010_09