HuagongsheHuagongshe Chemistry Print Report · For research reference only
Fluoroethane → Propanoyl fluoride, 3,3,3-trifluoro-2-(trifluoromethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Fluoroethane | HCID 9620 | — |
| Reactant | 1-Ethoxy-1,1,3,3,3-pentafluoro-2-(trifluoromethyl)propane | HCID 533655 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Catalyst | 3,3,3-Trifluoro-2-(trifluoromethyl)propionyl chloride | HCID 12809739 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Propanoyl fluoride, 3,3,3-trifluoro-2-(trifluoromethyl)- | HCID 181462 | 36.7% |
Reaction Steps
The above ethyl ether, 43 g (0.175 mol), in a 100 ml flask equipped as described in Example 6 was mixed with 1 g (0.0075 mol) of AlCl3. The mixture was refluxed for 17 hours. Material condensed in the attached Dry Ice-acetone trap was combined with residual material in the flask and distilled in a low-temperature still. An amount of 30.8 g of unreacted (CF3)2CHCF2OC2H5 was recovered, together with 9.1 g (26.3% yield) of (CF3)2CHCOF, 2.2 g of C2H5F and 0.1 g of (CF3)2CHCOCl. No improvement in product yield was obtained when the reactants were heated in a sealed tube at 120° for 4 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04357282 |
| Source dataset | uspto-grants-1982_11 |
| ORD ID | ord-a5fe1dae238441a19145063728062f47 |
| Source note | uspto-grants-1982_11 |