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HRID 6198생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물Benzaldehyde, 4-[[2-(acetyloxy)ethyl]ethylamino]-HCID 11458991—
반응물Tributyl(1,3-dioxolan-2-ylmethyl)phosphonium BromideHCID 22292430—
반응물Potassium tert-butoxideHCID 23665647—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물4-(N-2-hydroxyethyl-N-ethylamino)cinnamaldehydeHCID 54451596—

반응 조건

온도90 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05247042
출처 데이터셋uspto-grants-1993_09
ORD IDord-e8332f792cb943259f780b7e96c92708
출처 메모uspto-grants-1993_09