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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2173193Erstellt: 25. Oktober 2026

Trifluoroacetic acid → 5-bromo-4-fluoroisobenzofuran-1(3H)-one

https://huagongshe.com/reaction/2173193

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktLithium ChlorideHCID 433294—
EduktMagnesium monoxideHCID 6850729—
EduktThallium(1+);2,2,2-trifluoroacetateHCID 21902506—
Edukt3-Bromo-2-fluorobenzyl AlcoholHCID 26985646—
KatalysatorPalladium ChlorideHCID 24290—
LösungsmittelMethanolHCID 887—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-bromo-4-fluoroisobenzofuran-1(3H)-oneHCID 66644038—

Reaktionsschritte

To a flask charged with (3-bromo-2-fluorophenyl)methanol (840 mg, 4.1 mmol) and a stir bar was added added thallium trifluoroacetate (2.3 g, 4.3 mmol) and TFA (4.0 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 (73 mg, 0.41 mmol), lithium chloride (350 mg, 8.2 mmol), magnesium oxide (330 mg, 8.2 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 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-4-fluoro-2-benzofuran-1(3H)-one. LC-MS (IE, m/z): 231 [M+1]+;

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09056859B2
Quelldatensatzuspto-grants-2015_06
ORD IDord-82abb59f38284675984ad59b56281b47
Quellennotizuspto-grants-2015_06