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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 928674Erstellt: 25. Oktober 2026

Sodium Carbonate → 3-{[4-(4,5-Difluoro-1-benzofuran-7-yl)-phenoxy]methyl}benzoic acid

https://huagongshe.com/reaction/928674

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt1,4-DioxaneHCID 31275—
Edukt7-Bromo-4,5-difluorobenzofuranHCID 22144874—
Edukt3-{[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]methyl}benzoic acidHCID 90384406—
KatalysatorBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
LösungsmittelWaterHCID 962—
Produkt3-{[4-(4,5-Difluoro-1-benzofuran-7-yl)-phenoxy]methyl}benzoic acidHCID 90384393—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To the compound (1.67 g, 4.72 mmol) obtained in Step 1, 7-bromo-4,5-difluoro-1-benzofuran (1.1 g, 4.72 mmol), sodium carbonate (1.0 g, 9.44 mmol), and Pd(dppf)Cl2 (catalytic amount), 1,4-dioxane (24 mL) and water (8 mL) were added, and stirred at 100° C. for 2 hours. The reaction solution was concentrated under reduced pressure. To the residue, ethyl acetate and 1 N hydrochloric acid were added and stirred. After that, the insoluble material was filtered off, and extraction was performed with ethyl acetate. The organic phase was washed with saturated brine, and then dried over anhydrous magnesium sulfate. The solvent was distilled away under reduced pressure, and the solid was collected by filtration.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09290487B2
Quelldatensatzuspto-grants-2016_03
ORD IDord-bb37032e8f84428bb184d30e56bce31d
Quellennotizuspto-grants-2016_03