HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene carbonate → Phenyl Fluoroformate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene carbonate | HCID 7303 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Carbonochloridate | HCID 21226386 | — |
| Product | Phenyl Fluoroformate | HCID 11815898 | 93.5% |
Reaction Steps
The preparation was carried out as in Example 2 but using 250 g of ethylene carbonate, 89 g (1.53 mol) of potassium fluoride and 156.6 g (1.0 mol) of phenyl chloroformate. After addition of the chloroformate, stirring of the reaction mixture was continued at 45°-50° C. for 2 hours. Evaporation under vacuum was carried out as above. By distillation under reduced pressure, 131 g (93.5% yield) of phenyl fluoroformate with a boiling point of 62°-64° at 40 mm Hg were recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06613929B2 |
| Source dataset | uspto-grants-2003_09 |
| ORD ID | ord-eb37e1517b4743b8acccb02a295a296c |
| Source note | uspto-grants-2003_09 |