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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542299Generated: October 27, 2026

Hydrochloric Acid → Ethyl (3-aminobutyl)(diethoxymethyl)phosphinate

https://huagongshe.com/reaction/542299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantEthyl 3-oxobutyl(diethoxymethyl)phosphinateHCID 14362820—
SolventMethanolHCID 887—
ProductEthyl (3-aminobutyl)(diethoxymethyl)phosphinateHCID 14362822—

Reaction Steps

To a solution of 8.0 g of ethyl 3-oxobutyl(diethoxymethyl)phosphinate in 100 ml of methanol is added 22.8 g of ammonium acetate and 1.3 g of sodium cyanoborohydride. The mixture is stirred under an atmosphere of nitrogen at room temperature for a period of 2.5 h, and then left to stand overnight. The mixture is then acidified to pH 2 with the requisite amount of dilute hydrochloric acid and the methanol is evaporated under reduced pressure. The crude product is dissolved in 25 ml of water, washed twice with 20 ml of diethyl ether and the aqueous phase is then made alkaline to pH 12 with potassium hydroxide. The solution is then saturated with sodium chloride and extracted with 3×25 ml of dichloromethane. The organic phase is dried over magnesium sulphate, filtered and evaporated under reduced pressure and the crude product distilled to give ethyl 3-aminobutyl(diethoxymethyl)phosphinate, b.p. 150° C./0.01 mbar, 31P=+46.1 ppm (CDCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04656298
Source datasetuspto-grants-1987_04
ORD IDord-bbb5cf4121374153bd61759b09581164
Source noteuspto-grants-1987_04