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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6202Generated: October 26, 2026

Sodium Chloride → HCID 53997388, compound

https://huagongshe.com/reaction/6202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactant4-(N-4-acetoxybutyl-N-butylamino)benzaldehydeHCID 11011752—
ReactantTributyl(1,3-dioxolan-2-ylmethyl)phosphonium BromideHCID 22292430—
ReactantPotassium tert-butoxideHCID 23665647—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 53997388HCID 53997388—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 29.1 g (0.1 mole) of 4-(N-4-acetoxybutyl-N-butylamino)benzaldehyde in dimethylformamide is added 73.9 g (0.2 mole) of 1,3-dioxolan-2-ylmethyltributylphosphonium bromide in dimethylformamide, and the mixture is heated at 90° C. Potassium t-butoxide (22.4 g, 0.2 mole) is added, and heating is continued at 90° C. for 16 hours. After cooling to room temperature, the product solution is poured into a seven-fold excess of water, the aqueous mixture is saturated with sodium chloride and the solution is extracted with three portions of ether. The combined organics are dried over 4A sieves, filtered through cotton, and evaporated. The crude reaction product is then 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 passed through silica gel, dried over 4A sieves, filtered through cotton, and evaporated to yield compound A. 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-a8052ae73acf41bcbeb0aa54d437ed4a
Source noteuspto-grants-1993_09