Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 535675Erstellt: 24. Oktober 2026

Methyl chloroacetate → 7-Bromo-5-fluorobenzofuran-2-carboxylic acid

https://huagongshe.com/de/reaction/535675

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl chloroacetateHCID 7295—
EduktPotassium CarbonateHCID 11430—
EduktPotassium HydroxideHCID 14797—
Edukt3-Bromo-5-fluoro-2-hydroxybenzaldehydeHCID 23148955—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt7-Bromo-5-fluorobenzofuran-2-carboxylic acidHCID 1798270163%

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

Methyl chloroacetate (7.6 mL, 86.8 mmol) was added to a mixture of 3-bromo-5-fluoro-2-hydroxy-benzaldehyde (9.5 g, 43.4 mmol), tetra-N-butyl-ammonium iodide (1.6 g, 4.34 mmol) and anhydrous potassium carbonate (24 g, 174 mmol). The reaction mixture was heated at 130° C. for 4 h, cooled to 0° C., diluted with tetrahydrofuran (100 mL) and then potassium hydroxide (17 g, 303 mmol) in water (100 mL). The mixture was stirred at rt for 18 h and then, concentrated under reduced pressure. The residue was acidified with HCl and extracted with ethyl acetate. The combined organic extracts were dried (Na2SO4), filtered and concentrated under reduced pressure. The crude compound was purified by flash chromatography (SiO2; toluene/EtOAc, 40/1) to give 7.0 g (63%) of the product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08859534B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-5e519e47b4254bf38cafbd0db2f6a7ce
Quellennotizuspto-grants-2014_10