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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1780560Erstellt: 27. Oktober 2026

Dichloromethane → 1,4-Di(2-fluoro-6-octyloxypyridine-3-yl)benzene

https://huagongshe.com/reaction/1780560

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
Edukt1,4-DibromobenzeneHCID 7804—
EduktSodium CarbonateHCID 10340—
Edukt2-Fluoro-6-octyloxypyridine-3-boronic acidHCID 19046940—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelBenzeneHCID 241—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt1,4-Di(2-fluoro-6-octyloxypyridine-3-yl)benzeneHCID 1904694779,8%

Reaktionsschritte

0.87 g (3.7 mmol) of 1,4-dibromobenzene, 2.00 g (7.4 mmol) of 2-fluoro-6-octyloxypyridin-3-boronic acid (prepared as described in Example 5), 0.56 g (0.46 mmol) of tetrakis(triphenylphosphine)palladium(0) and 5 g (46.1 mmol) of sodium carbonate in 50 ml of benzene, 35 ml of ethanol and 20 ml of water are refluxed for 18 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, CH2Cl2) and recrystallization from acetonitrile give 1.55 g of 1,4-di(2-fluoro-6-octyloxypyridine-3-yl)benzene. ##STR36##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05630962
Quelldatensatzuspto-grants-1997_05
ORD IDord-a15a2e58252f4142aacc79a69cef98ad
Quellennotizuspto-grants-1997_05