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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 528588Erstellt: 23. Oktober 2026

Water → 4-Bromo-3'-Fluoro-3-Methoxy-1,1'-Biphenyl

https://huagongshe.com/de/reaction/528588

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt3-Fluorophenylboronic acidHCID 2733986—
Edukt1-Bromo-4-iodo-2-methoxybenzeneHCID 12187202—
KatalysatorHCID 178418807HCID 178418807—
LösungsmittelDichloromethaneHCID 6344—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt4-Bromo-3'-Fluoro-3-Methoxy-1,1'-BiphenylHCID 89762084—

Reaktionsschritte

A solution of PdCl2(dppf)-CH2Cl2 adduct (0.065 g, 0.080 mmol), 1-bromo-4-iodo-2-methoxybenzene (CombiBlocks, 0.250 g, 0.799 mmol), 3-fluorophenylboronic acid (0.123 g, 0.879 mmol) and potassium phosphate (0.848 g, 3.99 mmol) in dioxane (2.130 ml)/water (1.065 ml) was heated to 90° C. overnight. The reaction was diluted with DCM and separated from the aqueous via phase separator (Radleys Discovery Technologies). After concentration in vacuo, the material was purified via MPLC (12-g Redi Sep Gold), eluting with 0-100% ethyl acetate in heptanes to yield, after concentration, 4-bromo-3′-fluoro-3-methoxy-1,1′-biphenyl as an orange oil, which was used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09346798B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-a2cb8c1e3c1c4b5f8dc08dffba635e8a
Quellennotizuspto-grants-2016_05