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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492966Generated: October 26, 2026

Acetic Acid → 3-(3,5-Dichloro-benzylamino)propyl(diethoxymethyl)phosphinic acid ethyl ester

https://huagongshe.com/reaction/1492966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3,5-DichlorobenzaldehydeHCID 35746—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantPhosphinic acid, (3-aminopropyl)(diethoxymethyl)-, ethyl esterHCID 10422382—
SolventMethanolHCID 887—
Product3-(3,5-Dichloro-benzylamino)propyl(diethoxymethyl)phosphinic acid ethyl esterHCID 21805327—

Reaction Steps

1.41 g of 3,5-dichlorobenzaldehyde 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 dissolved in 5 ml of methanol. An exothermic reaction begins. The reaction mixture is stirred for 3 hours at 20°, 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 behind is purified by chromatography on silica gel, yielding 3-(3,5-dichlorobenzylamino)propyl(diethoxymethyl)-phosphinic acid ethyl ester in the form of a yellowish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05376684
Source datasetuspto-grants-1994_12
ORD IDord-4d12480d8cbd4fafae5b653b79656c24
Source noteuspto-grants-1994_12