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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1780559Erstellt: 26. Oktober 2026

Dichloromethane → 2-Fluoro-6-octyloxy-3-[4-(4-octyloxyphenyl)phenyl]pyridine

https://huagongshe.com/reaction/1780559

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktSodium CarbonateHCID 10340—
Edukt1-Bromo-4-(4-octoxyphenyl)benzeneHCID 2801787—
Edukt2-Fluoro-6-octyloxypyridine-3-boronic acidHCID 19046940—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelBenzeneHCID 241—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt2-Fluoro-6-octyloxy-3-[4-(4-octyloxyphenyl)phenyl]pyridineHCID 1904697313,2%

Reaktionsschritte

2.10 g (7.50 mmol) of 2-fluoro-6-octyloxypyridine-3-boronic acid (prepared as described in Example 5) in 35 ml of ethanol are refluxed together with 2.70 g (7.50 mmol) of 4-bromo-4'-octyloxybiphenyl and 0.29 g (0.24 mmol) of tetrakis(triphenylphosphine)palladium in 46 ml of benzene and 2.5 g (23.40 mmol) of sodium carbonate in 11 ml of water for 20 hours. After distributing the reaction mixture between water and dichloromethane, the organic phase is washed with sodium chloride solution, dried over sodium sulfate, filtered and concentrated. Purification of the residue by chromatography (silica gel, dichloromethane) and recrystallization from acetonitrile give 0.50 g of 2-fluoro-6-octyloxy-3-[4-(4-octyloxyphenyl)phenyl]pyridine. ##STR32##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05630962
Quelldatensatzuspto-grants-1997_05
ORD IDord-51874d2e1e3549caa257c4049dcb364b
Quellennotizuspto-grants-1997_05