HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,2-Trifluoroethanol → 2-(2,2,2-Trifluoroethoxy)ethan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | Ethylene carbonate | HCID 7303 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Product | 2-(2,2,2-Trifluoroethoxy)ethan-1-ol | HCID 255854 | 61% |
Reaction Steps
2,2,2-Trifluoroethanol (10.0 g, 0.10 mol), triethylamine (10.1g, 0.10 mol), ethylene carbonate (13.2 g, 0.15 mol) and tetrabutyl ammonium iodide (0.74 g) were heated in a flask fitted with a reflux condenser under nitrogen in an oil bath at 100° C. for 1 day. The triethylamine and unreacted alcohol were removed by distillation. The product 2-(2,2,2-trifluoroethoxy)ethanol, b.p. 138° C., was obtained in 61% yield (8.6 g) of 97% pure material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05157159 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-8f61e9721d4441aba2d17d72b8a13361 |
| Source note | uspto-grants-1992_10 |