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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542301Generated: October 25, 2026

Acetic Acid → Ethyl 1-(4-chlorophenyl)-2-cyanoethyl(diethoxymethyl)phosphinate

https://huagongshe.com/reaction/542301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium hydrideHCID 24758—
Reactant3-(4-Chlorophenyl)prop-2-enenitrileHCID 34243—
ReactantEthyl(diethoxymethyl)phophoniteHCID 85631043—
SolventEthanolHCID 702—
ProductEthyl 1-(4-chlorophenyl)-2-cyanoethyl(diethoxymethyl)phosphinateHCID 14362807—

Reaction Steps

The starting material may be prepared as follows: A solution of 25.8 g of ethyl(diethoxymethyl)phosphonite and 18.0 g of 4-chlorocinnamonitrile in 100 ml of ethanol is added to a stirred mixture of 1.2 g of sodium hydride (50% dispersion in oil) in 30 ml of ethanol at 0° C. under an atmosphere of nitrogen. The reaction mixture is allowed to warm to room temperature and stirred for 4 hours. 1 ml of glacial acetic acid is added and the mixture is concentrated under reduced pressure. The resulting crude product is dissolved in 50 ml of ethyl acetate, washed twice with 25 ml of water and the organic extract is dried over magnesium sulphate, and then concentrated under reduced pressure. The crude product is distilled under reduced pressure to give ethyl 1-(4-chlorophenyl)-2-cyanoethyl(diethoxymethyl)phosphinate, b.p. 180°-200° C./0.02 mbar, 31P=+37.9 and +37.8 ppm (CDCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04656298
Source datasetuspto-grants-1987_04
ORD IDord-2c53bce63d364e14ae897a2cbb6c1e75
Source noteuspto-grants-1987_04