HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorodifluoromethane → Ethyl 1,1-diethoxyethyl(difluoromethyl)phosphinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorodifluoromethane | HCID 6372 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178476820 | HCID 178476820 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 1,1-diethoxyethyl(difluoromethyl)phosphinate | HCID 9992738 | — |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05300679 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-c0c74fdc3111405993a7c37851007486 |
| Source note | uspto-grants-1994_04 |