Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl trifluoroacetateHCID 9794—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant1-(5-Bromofuran-2-yl)ethan-1-oneHCID 11030585—
SolventTetrahydrofuranHCID 8028—
Product1-(5-Bromofuran-2-yl)-4,4,4-trifluorobutane-1,3-dioneHCID 8978287669.1%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987318B2
Source datasetuspto-grants-2015_03
ORD IDord-401fb6608b5e42a7a84bd757da1a8647
Source noteuspto-grants-2015_03