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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654460Generated: November 1, 2026

Acetic Acid → 3-(p-Chlorobenzylamino)propyl(diethoxymethyl)phosphinic acid ethyl ester

https://huagongshe.com/reaction/1654460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantPhosphinic acid, (3-aminopropyl)(diethoxymethyl)-, ethyl esterHCID 10422382—
SolventMethanolHCID 887—
Product3-(p-Chlorobenzylamino)propyl(diethoxymethyl)phosphinic acid ethyl esterHCID 54432946—

Reaction Steps

1.41 g of p-chlorobenzaldehyde are added to a solution of 2.53 g of 3-aminopropyl(diethoxymethyl)phosphinic acid ethyl ester in 10 ml of anhydrous methanol, and the resulting clear solution is stirred at room temperature for 30 minutes. There are then added first 0.6 g of glacial acetic acid and then, dropwise, 0.21 g of sodium cyanoborohydride in solution in 5 ml of methanol. An exothermic reaction begins. The mixture is stirred at 20° for 3 hours and adjusted to pH 8, and the solvent is removed. The residue is dissolved in dichloromethane and washed with water. The organic phase is separated off, dried over sodium sulfate and concentrated to dryness by evaporation. The oil that remains is purified by chromatography on silica gel, yielding 3-(p-chlorobenzylamino)propyl(diethoxymethyl)phosphinic acid ethyl ester in the form of a yellowish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05407922
Source datasetuspto-grants-1995_04
ORD IDord-cbf4d35225724309a4ecd290c1a8eb7d
Source noteuspto-grants-1995_04