HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877451Generated: October 29, 2026
Ethyl trifluoroacetate → 1-(5-Bromofuran-2-yl)-4,4,4-trifluorobutane-1,3-dione
https://huagongshe.com/reaction/877451
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 1-(5-Bromofuran-2-yl)ethan-1-one | HCID 11030585 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(5-Bromofuran-2-yl)-4,4,4-trifluorobutane-1,3-dione | HCID 89782876 | 69.1% |
Reaction Steps
To a stirred solution of compound 43 (4.8 g, 25.4 mmol) in THF (60 mL) at −78° C., LiHMDS (38 mL, 38.1 mmol) was added dropwise and the reaction stirred −78° C. for 1 h. Ethyl 2,2,2-trifluoroacetate (4.5 g, 38.1 mmol) was then added dropwise. The reaction mixture was allowed to gradually warm to room temperature in cooling bath and stirred overnight. Solvent was removed, cold water (50 mL) was added, and the reaction mixture extracted with diethyl ether (100 mL×3). Combined organic layer was washed with brine, dried over sodium sulphate and concentrated under reduced pressure. Crude compound was washed with diethyl ether and hexane to afford compound 44 (5 g, 69%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987318B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-401fb6608b5e42a7a84bd757da1a8647 |
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| Source note | uspto-grants-2015_03 |
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