Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077699Generated: October 31, 2026

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

https://huagongshe.com/reaction/1077699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-Aminopropyl(n-butyl)phosphinic acid ethyl esterHCID 9990598—
SolventMethanolHCID 887—
Product3-(p-Chlorobenzylamino)propyl(n-butyl)phosphinic acid ethyl esterHCID 53755720—

Reaction Steps

4.14 g of 3-aminopropyl(n-butyl)phosphinic acid ethyl ester are mixed with 2.51 g of p-chlorobenzaldehyde, and first 1.2 g of glacial acetic acid and then a solution of 0.42 g of sodium cyanoborohydride in 5 ml of methanol are added, whereupon an exothermic reaction takes place. The mixture is then stirred at room temperature for 2.5 hours and adjusted to pH 8, and the volatile constituents are removed under reduced pressure. The residue is dissolved in dichloromethane, washed with water, dried over sodium sulfate and concentrated by evaporation. The residue is purified by chromatography on silic gel, yielding 3-(p-chlorobenzylamino)propyl(n-butyl)phosphinic acid ethyl ester; 1H--NMR spectrum (in CDCl3): δ=7.30-7.32 (4H,m); 4.02 (2H,q); 3.74 (2H,s); 2.67 (2H,t); 2.5-2.2 (1H,S); 1.79-1.64 (6H,m); 1.53 (2H,m); 1.42 (2H,m); 1.31 (3H,t); 0.81 (3H,t); 31P--NMR spectrum (in CDCl3); δ=58.16.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05545631
Source datasetuspto-grants-1996_08
ORD IDord-54056f2c33f54be2ae20168cf5cd40c2
Source noteuspto-grants-1996_08