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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622884Generated: October 31, 2026

Hydrochloric Acid → Ethyl 3-amino-3-(4-chlorophenyl)propyl(diethoxymethyl)phosphinate

https://huagongshe.com/reaction/622884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantEthyl 2-(4-chlorobenzoyl)ethyl(diethoxymethyl)phosphinateHCID 14362821—
SolventMethanolHCID 887—
ProductEthyl 3-amino-3-(4-chlorophenyl)propyl(diethoxymethyl)phosphinateHCID 14362823—

Reaction Steps

To a solution of 25.4 g of ethyl 2-(4-chlorobenzoyl)ethyl(diethoxymethyl)phosphinate in 200 ml of methanol is added 52 g of ammonium acetate and 4.23 g of sodium cyanoborohydride. The mixture is stirred under an atmosphere of nitrogen at room temperature for a period of 3 days. 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 layer 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 and then evaporated under reduced pressure to give ethyl 3-amino-3-(4-chlorophenyl)propyl(diethoxymethyl)phosphinate as a viscous oil, 31P=45.9 ppm (CDCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04772738
Source datasetuspto-grants-1988_09
ORD IDord-0bc9ac79ac2141158d4062b4917b37ff
Source noteuspto-grants-1988_09