HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Ether → 2,3,3,3-Tetrafluoropropanoyl fluoride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Ether | HCID 8254 | — |
| Reactant | Hexafluoropropylene | HCID 8302 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,3,3,3-Tetrafluoropropanoyl fluoride | HCID 13319073 | 82% |
Reaction Steps
The above methyl ether (49.5 g, prepared from the reaction of hexafluoropropene with sodium methoxide in methanol) in a still pot was cooled in a Dry Ice-acetone bath and 2.70 g of SbF5 was added. The mixture was stirred on a still with a Dry Ice-acetone trap attached and the cooling bath removed. Evolution of CH3F was vigorous below room temperature. The mixture was warmed until all of the product had collected in the Dry Ice-acetone trap. Material in the trap was redistilled in a low-temperature still to give 33 g (82%) of 2,3,3,3-tetrafluoropropionylfluoride, b.p. 25°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04357282 |
| Source dataset | uspto-grants-1982_11 |
| ORD ID | ord-bf09462b33aa47aba1da2834c7b2c543 |
| Source note | uspto-grants-1982_11 |