HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366365Generated: October 31, 2026
Ethyl trifluoroacetate → 1-[4-(Benzyloxy)phenyl]-4,4,4-trifluorobutane-1,3-dione
https://huagongshe.com/reaction/1366365
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 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 1 N 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 |
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| Patent number | US07893057B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-426af1ae24374c0eb56015b80d306be0 |
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| Source note | uspto-grants-2011_02 |
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