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HRID 6198作成日:2026年10月25日

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

https://huagongshe.com/reaction/6198

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物Benzaldehyde, 4-[[2-(acetyloxy)ethyl]ethylamino]-HCID 11458991—
反応物Tributyl(1,3-dioxolan-2-ylmethyl)phosphonium BromideHCID 22292430—
反応物Potassium tert-butoxideHCID 23665647—
溶媒Hydrochloric AcidHCID 313—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物4-(N-2-hydroxyethyl-N-ethylamino)cinnamaldehydeHCID 54451596—

反応条件

温度90 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05247042
出典データセットuspto-grants-1993_09
ORD IDord-e8332f792cb943259f780b7e96c92708
出典メモuspto-grants-1993_09