HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexafluoroacetone → CH2=C(CF3)CF2Ocf(CF3)2
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexafluoroacetone | HCID 12695 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | CH2=C(CF3)CF2Oso2F | HCID 87741755 | — |
| Reactant | HCID 178506340 | HCID 178506340 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | CH2=C(CF3)CF2Ocf(CF3)2 | HCID 131726622 | 75% |
Reaction Steps
CH2═C(CF3)CF2OSO2F (10 g, 0.041 mole) is added at 20° C. to (CF3)2CFOK, prepared from freshly dried potassium fluoride (KF) (2.4 g, 0.041 mole), hexafluoroacetone (HFA) (9.3 g, 0.056 mole) and dry diglyme (10 ml). The reaction mixture is agitated for 2 hours and then poured into water, the organic layer separating. The organic layer is washed with dilute hydrochloric acid, then sodium bicarbonate solution, then water, after which it is dried over magnesium sulfate (MgSO4). Distillation of the reaction mixture gives CH2═C(CF3)CF2OCF(CF3)2 (10.2 g, 75% yield, b.pt. 87-88° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531689B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-61bbb6880b5848b48f20d230a18363c6 |
| Source note | uspto-grants-2009_05 |