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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 269591Erstellt: 23. Oktober 2026

Hydrochloric Acid → 6''Fluoro-2-benzyloxy-[1,1':2',1'']terphenyl-3''-carboxylic acid

https://huagongshe.com/de/reaction/269591

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPotassium CarbonateHCID 11430—
Edukt3-Bromo-4-fluorobenzoic acidHCID 70509—
Edukt2'-Benzyloxy-biphenyl-2-boronic acidHCID 58730990—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt6''Fluoro-2-benzyloxy-[1,1':2',1'']terphenyl-3''-carboxylic acidHCID 44581655—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

{2′-[(phenylmethyl)oxy]-2-biphenylyl}boronic acid (60 mg, 0.19 mmol) and 3-bromo-4-fluorobenzoic acid (69 mg, 0.31 mmol) were dissolved in 1:1 toluene:ethanol (6 ml) under nitrogen. Potassium carbonate (290 mg, 2.1 mmol) and tetrakis(triphenylphosphine)palladium(0) (23 mg, 0.019 mmol) were added and the mixture heated at 90° C. for 1 h. After cooling, the reaction mixture was poured into water, acidified with 1M HCl solution and extracted with ethyl acetate (15×2 ml), the combined organic layer were dried and evaporated. The residue was then purified on an SPE column using 40% of ethyl acetate in iso-hexane to give the title compound as white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07446222B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-87b199b644b94a979230c2456be54945
Quellennotizuspto-grants-2008_11