HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl trifluoroacetate → 1-[4-(Benzyloxy)phenyl]-4,4,4-trifluorobutane-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | 1-[4-(Benzyloxy)phenyl]ethan-1-one | HCID 245226 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[4-(Benzyloxy)phenyl]-4,4,4-trifluorobutane-1,3-dione | HCID 21894454 | 100% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
45.2 g 1-(4-Benzyloxy-phenyl) ethanone (200 mmol) was taken up in THF (250 mL) and treated with CF3CO2Et (30 ml, 250 mmol). The solution was cooled to 0° C. and treated with 2.66 M NaOEt (94 ml, 250 mmol) solution over 1 h. The ice bath was removed and the solution was stirred at room temperature for 4 h. The reaction was poured into 1N HCl (1000 ml) and extracted with EtOAc (1500 ml). The organic layer was washed with brine, dried and evaporated to yield 64.2 g 1-(4-Benzyloxy-phenyl)-4,4,4-trifluoro-butane-1,3-dione (200 mmol, 100% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135550B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-f879d593cf6f4429beb878e39beaeca6 |
| Source note | uspto-grants-2006_11 |