Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 53942597 | HCID 53942597 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19090879 | HCID 19090879 | — |
Reaction Steps
A solution of sodium ethoxide in absolute ethanol (0.48 g of sodium metal in 15 ml of absolute ethanol) is cooled to 0° under nitrogen or argon. A solution of 2.72 g of acrylonitrile and 12.2 g of di-n-propyloxymethylphosphonous acid n-propylester in 50 ml of absolute ethanol is added at such a rate that the temperature does not exceed 5°. After the addition is completed, the solution is allowed to warm to room temperature and stirred overnight. After addition of 1.22 g of glacial acetic acid, the reaction mixture is concentrated in vacuo. Theresidue is partitioned between ethyl acetate and water and the organic phase separated. After drying over anhydrous magnesium sulphate the solvent is evaporated in vacuo to afford an oil. Chromatography on silica-gel yields ethyl 2-cyanoethyl(di-n-propyloxymethyl)phosphinate as acolourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05051524 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-b5804bc4385842f9ba0676cd4918a57f |
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| Source note | uspto-grants-1991_09 |
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