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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6198Generated: October 25, 2026

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

https://huagongshe.com/reaction/6198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantBenzaldehyde, 4-[[2-(acetyloxy)ethyl]ethylamino]-HCID 11458991—
ReactantTributyl(1,3-dioxolan-2-ylmethyl)phosphonium BromideHCID 22292430—
ReactantPotassium tert-butoxideHCID 23665647—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-(N-2-hydroxyethyl-N-ethylamino)cinnamaldehydeHCID 54451596—

Reaction Conditions

Temperature90 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05247042
Source datasetuspto-grants-1993_09
ORD IDord-e8332f792cb943259f780b7e96c92708
Source noteuspto-grants-1993_09