HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Chlorodifluoromethane → Ethyl 1,1-diethoxyethyl(difluoromethyl)phosphinate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Chlorodifluoromethane | HCID 6372 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | HCID 178476820 | HCID 178476820 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Ethyl 1,1-diethoxyethyl(difluoromethyl)phosphinate | HCID 9992738 | — |
Reaktionsschritte
To a suspension of 15.8 g of sodium hydride (dispersion in oil) in 500 ml of tetrahydrofuran are added dropwise 67 g (300 mMol) of ethyl 1,1-diethoxyethylphosphinate at such a rate so that the temperature does not exceed 25° C. This mixture is stirred for one hour at room temperature, then cooled to -10° C. and 77.8 g (900 mMol) of chlorodifluoromethane are introduced. Stirring is continued for another 2 hours at room temperature, then 100 ml of ice-cold water are added. The mixture is extracted three times with dichloromethane and the combined extracts dried over magnesium sulphate. Removal of the solvent in vacuo gives ethyl 1,1-diethoxyethyl(difluoromethyl)phosphinate as a viscous oil,Rf=0.44 (CH2Cl2 /CH3COOH, 9+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05051524 |
| Quelldatensatz | uspto-grants-1991_09 |
| ORD ID | ord-02fe391efa80496fa3c2b41223b9a2b8 |
| Quellennotiz | uspto-grants-1991_09 |