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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173196Generated: October 29, 2026

Trifluoroacetic acid → HCID 66643914, compound

https://huagongshe.com/reaction/2173196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantLithium ChlorideHCID 433294—
Reactant(3-Bromo-5-fluorophenyl)methanolHCID 2769402—
ReactantMagnesium monoxideHCID 6850729—
ReactantThallium(1+);2,2,2-trifluoroacetateHCID 21902506—
CatalystPalladium ChlorideHCID 24290—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 66643914HCID 66643914—

Reaction Steps

To a flask charged with (3-bromo-5-fluorophenyl)methanol (360 mg, 1.8 mmol) and a stir bar was added added thallium trifluoroacetate (1.0 g, 1.8 mmol) and TFA (3.0 mL) at 0° C. The mixture was allowed to stir for 16 hours. LC showed no SM left at that point. The volatiles were removed under reduced pressure, and the residue was dissolved in DCM and concentrated twice to affect azeotropic removal of all TFA. After pumping the residue under high vacuum for 20 minutes, palladium chloride (31 mg, 0.18 mmol), lithium chloride (150 mg, 3.5 mmol), magnesium oxide (140 mg, 3.5 mmol), and MeOH (15 mL) were added to the flask. The mixture was treated under an atmosphere of CO for 2 hours. To this mixtue was added DCM and EtOAc to precipitate all the inorganic solids. The crude solution was filtered through a Celite® pad, and the filtrate was collected, adsorbed onto silica gel, and purified by silica gel chromatography. Removal of solvents gave rise to 5-bromo-7-fluoro-2-benzofuran-1(3H)-one. LC-MS (IE, m/z): 231 [M+1]+;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-8007b76971834ef6bdc58c1a24f24e2b
Source noteuspto-grants-2015_06