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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1186925Erstellt: 26. Oktober 2026

Trifluoroacetic acid → 5-Bromo-4-methylisobenzofuran-1(3H)-one

https://huagongshe.com/reaction/1186925

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktLithium ChlorideHCID 433294—
EduktMagnesium monoxideHCID 6850729—
Edukt(3-Bromo-2-methylphenyl)methanolHCID 10035697—
EduktThallium(1+);2,2,2-trifluoroacetateHCID 21902506—
KatalysatorPalladium ChlorideHCID 24290—
LösungsmittelMethanolHCID 887—
Produkt5-Bromo-4-methylisobenzofuran-1(3H)-oneHCID 59568711—

Reaktionsschritte

To a flask charged with (3-bromo-2-methylphenyl)methanol (6.0 g, 30 mmol) was added a 1M TFA solution of Thallium Trifluoroacetate (16.2 g, 29.8 mmol). The mixture was stirred at RT overnight. Analysis by TLC showed no starting material remaining. The solvent was removed under vacuum, and the residue was pumped under high vacuum for 30 min to ensure complete removal of TFA. To the residue was then added Palladium(II) Chloride (529 mg, 2.98 mmol), Lithium Chloride (2.53 g, 59.7 mmol), Magnesium Oxide (2.41 g, 59.7 mmol), and MeOH (150 mL). The reaction was flushed with CO twice, and kept under CO at room temperature. Analysis by LC showed a big product spot within 2 hours. To this solution was added ethyl acetate to precipitate the salts. The black solution was filtered through a celite pad, washed with EtOAc, adsorbed onto silica and purified by silica gel chromatography to afford 5-bromo-4-methyl-2-benzofuran-1(3H)-one.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08673920B2
Quelldatensatzuspto-grants-2014_03
ORD IDord-708fa29ce039401eb2cb034778ecfbfa
Quellennotizuspto-grants-2014_03