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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043318Generated: November 1, 2026

Cesium fluoride → HCID 24825943, compound

https://huagongshe.com/reaction/2043318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
Reactant3-(Trifluoromethyl)phenylboronic acidHCID 2734388—
Reactant5-(Bromomethylidene)furan-2(5H)-oneHCID 67228360—
CatalystTetrabutylammonium IodideHCID 67553—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 24825943HCID 24825943—

Reaction Steps

A mixture containing 5-bromomethylene-2(5H)furanone (0.175 g, 1 mmol), 3-trifluoromethylphenylboronic acid (0.228 g, 1.2 mmol), trans-dichlorobis(triphenylphosphine)palladium (II) (0.035 g, 0.05 mmol), tetrabutylammonium iodide (0.018 g, 0.05 mmol) and cesium fluoride (0.456 g, 3 mmol) in toluene (10 mL) and water (10 mL) were stirred at reflux for 24 hours under nitrogen. After cooling, brine (50 mL) was added and the product extracted with ethyl acetate (50 mL×3). The organic fractions were combined, washed with brine (50 mL×3), dried over anhydrous sodium sulfate and evaporated to dryness to give a brown solid. The resulting solid was chromatographed (silica gel: eluent 50:50 dichloromethane/light petroleum) giving the desired product 30 as a light brown powder. Yield 0.180 g (75%), m.p. 69-71° C., UV-Vis λmax (MeOH) 223 (15166), 323 (31738) nm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586618B2
Source datasetuspto-grants-2013_11
ORD IDord-3c1bf9c1b6994f01b699a1611e2b9124
Source noteuspto-grants-2013_11