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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654471Generated: October 30, 2026

Acetic Acid → 3-(p-Chlorobenzylamino)propyl(tetrahydrofuran-2-yl)phosphinic acid ethyl ester

https://huagongshe.com/reaction/1654471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-(p-Chlorobenzylamino)propyl(diethoxymethyl)phosphinic acid ethyl esterHCID 54432946—
SolventMethanolHCID 887—
Product3-(p-Chlorobenzylamino)propyl(tetrahydrofuran-2-yl)phosphinic acid ethyl esterHCID 54448003—

Reaction Steps

2.5 g of 3-(p-chlorobenzylamino)propyl(diethoxymethyl)phosphinic acid ethyl ester are dissolved in 10 ml of methanol, 0.36 g (0.53 ml)of a 35% aqueous formaldehyde solution is added, and the mixture is stirred at room temperature for one hour. 0.4 g of glacial acetic acid and 0.40 g of sodium cyanoborohydride are added, and the mixture is stirred at room temperature for 2 hours, concentrated by evaporation under reduced pressure, taken up in dichloromethane and washed with 5% aqueous sodium hydrogen carbonate solution. The organic phase is separated off, dried over sodium sulfate and concentrated by evaporation under reduced pressure. The oily residue is purified by chromatography on silica gel, yielding 3-(p-chlorobenzylamino)propyl(tetrahydrofuran-2-yl)phosphinic acid ethyl ester in the form of a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05407922
Source datasetuspto-grants-1995_04
ORD IDord-7e911492944240db9b31d58e1d151f59
Source noteuspto-grants-1995_04