HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865834Generated: October 30, 2026
Acetic Acid → isobutyl P-(2-cyanoethyl)-P-methyl-phosphinate
https://huagongshe.com/reaction/865834
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Isobutyl methanephosphonite | HCID 86741778 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | isobutyl P-(2-cyanoethyl)-P-methyl-phosphinate | HCID 2304642 | — |
Reaction Steps
A solution of 15.0 g of isobutyl P-methylphosphonite and 5.3 g of acrylonitrile in 50 ml of dry ethanol is added to a stirred mixture of 0.5 g of sodium (50% dispersion in oil) in 25 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 20 ml of water, and the organic extract is dried over magnesium sulphate, and then concentrated under reduced pressure. The crude product is distilled to give isobutyl P-(2-cyanoethyl)-P-methyl-phosphinate, b.p. 140°/0.2 mbar, 31P-NMR spectrum: δ=+50.5 ppm (CDCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05567840 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-efffefb8c1944c609c93566c82b58afc |
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| Source note | uspto-grants-1996_10 |
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