HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,2-Trifluoroethanol → CH2=C(CF3)CF2Och2CF3
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | CH2=C(CF3)CF2Oso2F | HCID 87741755 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | CH2=C(CF3)CF2Och2CF3 | HCID 85887659 | 30% |
Reaction Steps
A 100 ml flask is charged with tributylamine (15 g), diglyme (20 ml) in a dry box. 2,2,2-Trifluoroethanol (8.05 g) is added to the mixture. CH2═C(CF3)CF2OSO2F (19.5 g) is added dropwise while the mixture is cooled in an ice-water bath. The resulting mixture is stirred at room temperature for 3 hours. The mixture is then distilled to give a liquid, which is redistilled (spinning band column) giving 5.8 g CH2═C(CF3)CF2OCH2CF3, b.pt. 85-86° C., a yield of 30%. Less pure fractions are not included in the yield calculation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07579499B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-bae00d6c3e2f498faa8ef0e2fffd855f |
| Source note | uspto-grants-2009_08 |