HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622880Generated: October 25, 2026
Acetic Acid → Ethyl 1-(4-chlorophenyl)-2-cyanoethyl(diethoxymethyl)phosphinate
https://huagongshe.com/reaction/622880
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(4-Chlorophenyl)prop-2-enenitrile | HCID 34243 | — |
| Reactant | Ethyl(diethoxymethyl)phophonite | HCID 85631043 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 1-(4-chlorophenyl)-2-cyanoethyl(diethoxymethyl)phosphinate | HCID 14362807 | — |
Reaction Steps
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04772738 |
|---|
| Source dataset | uspto-grants-1988_09 |
|---|
| ORD ID | ord-171b3d1675df4d76876714b9a04b5216 |
|---|
| Source note | uspto-grants-1988_09 |
|---|