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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1780067Erstellt: 26. Oktober 2026

Ethanol → 3-Chloro-2,5-di(4-octyloxyphenyl)pyridine

https://huagongshe.com/reaction/1780067

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktSodium CarbonateHCID 10340—
Edukt4-n-Octyloxyphenylboronic Acid (contains varying amounts of Anhydride)HCID 3977284—
Edukt5-Bromo-3-chloro-2-(4-octyloxyphenyl)pyridineHCID 19050004—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt3-Chloro-2,5-di(4-octyloxyphenyl)pyridineHCID 1904999348,9%

Reaktionsschritte

2.00 g (5.40 mmol) of 5-bromo-3-chloro-2-(4-octyloxyphenyl)pyridine, 1.50 g (6.00 mmol) of 4-octyloxybenzeneboronic acid, 0.07 g (0.6 mmol) of tetrakis(triphenylphosphine)palladium(0) and 1.3 g (12.00 mmol) of sodium carbonate are heated at 80° C. for 3 hours in 20 ml of toluene, 10 ml of ethanol and 10 ml of water. The mixture is subsequently partitioned between aqueous sodium chloride solution and ether, the organic phase is washed with aqueous sodium chloride solution, dried over sodium sulfate and evaporated, and the product is purified by chromatography (silica gel/dichloromethane), giving 1.38 g of 3-chloro-2,5-di(4-octyloxyphenyl)pyridine. ##STR24##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05629428
Quelldatensatzuspto-grants-1997_05
ORD IDord-6369c675c53c486b9e2852c43191dc58
Quellennotizuspto-grants-1997_05