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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6198Erstellt: 23. Oktober 2026

Sodium Chloride → 4-(N-2-hydroxyethyl-N-ethylamino)cinnamaldehyde

https://huagongshe.com/de/reaction/6198

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ChlorideHCID 5234—
EduktBenzaldehyde, 4-[[2-(acetyloxy)ethyl]ethylamino]-HCID 11458991—
EduktTributyl(1,3-dioxolan-2-ylmethyl)phosphonium BromideHCID 22292430—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(N-2-hydroxyethyl-N-ethylamino)cinnamaldehydeHCID 54451596—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a solution of 235.3 g (1 mole) of 4-(N-2-acetoxyethyl-N-ethylamino)benzaldehyde in dimethylformamide is added 738.7 g (2.0 moles) of 1,3-dioxolan-2-ylmethyltributylphosphonium bromide in dimethylformamide, and the mixture is heated at 90° C. Potassium t-butoxide (224.4 g, 2.0 moles) is added, and heating is continued at 90° C. for 16 hours. After cooling to room temperature, the solution is poured into a seven-fold excess of water, the aqueous mixture is saturated with sodium chloride, The combined organics are dried over 4A sieves, filtered through cotton, and evaporated. The crude reaction product is dissolved in 3M HCl, and the reaction is stirred at room temperature for 16 hours. After neutralization with saturated sodium bicarbonate, the aqueous mixture is extracted with three portions of ether, and the combined organics are dried over 4A sieves, filtered through cotton, and evaporated to yield the cinnamaldehyde as an oil. The product is purified by flash chromatography (silica gel, 1:1 hexane:ethyl acetate).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05247042
Quelldatensatzuspto-grants-1993_09
ORD IDord-e8332f792cb943259f780b7e96c92708
Quellennotizuspto-grants-1993_09