HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 542291Erstellt: 25. Oktober 2026
Acetic Acid → Ethyl 2-cyanoethyl(diethoxymethyl)phosphinate
https://huagongshe.com/reaction/542291
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Acrylonitrile | HCID 7855 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Ethyl(diethoxymethyl)phophonite | HCID 85631043 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Ethyl 2-cyanoethyl(diethoxymethyl)phosphinate | HCID 10037677 | — |
Reaktionsschritte
The starting material can be prepared as follows: A solution of 20 g of ethyl(diethoxymethyl)phosphonite (Aust. J. Chem. 33, 292 (1980)) and 5 g of acrylonitrile in 25 ml of ethanol is added to a stirred mixture of 1 g of sodium hydride (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 26 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 2-cyanoethyl(diethoxymethyl)phosphinate, b.p. 114° C./0.01 mbar, 31P=+40.8 ppm (CDCl3).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04656298 |
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| Quelldatensatz | uspto-grants-1987_04 |
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| ORD ID | ord-f260520ff0694acea23e672735633670 |
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| Quellennotiz | uspto-grants-1987_04 |
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