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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1780553Erstellt: 27. Oktober 2026

Ethanol → 2-Fluoro-6-octyloxy3-(4-octyloxyphenyl)pyridine

https://huagongshe.com/reaction/1780553

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktSodium CarbonateHCID 10340—
Eduktp-Bromophenyl octyl etherHCID 145298—
Edukt2-Fluoro-6-octyloxypyridine-3-boronic acidHCID 19046940—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelBenzeneHCID 241—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
Produkt2-Fluoro-6-octyloxy3-(4-octyloxyphenyl)pyridineHCID 1904696941,5%

Reaktionsschritte

2.00 g (7.44 mmol) of 2-fluoro-6-octyloxypyridine-3-boronic acid, 1.64 g (5.72 mmol) of 1-bromo-4-octyloxybenzene, 0.26 g (0.22 mmol) of tetrakis(triphenylphosphine)palladium(0) and 11.16 ml (22.32 mmol) of 2-molar sodium carbonate solution are refluxed in 20 ml of benzene and 10 ml of ethanol for 6 hours. After distributing the reaction mixture between water and diethyl ether, the organic phase is washed with water, dried over sodium sulfate, filtered and concentrated. Purification of the residue by chromatography (silica gel, 95:5 hexane/ethyl acetate) and recrystallization from acetonitrile give 1.02 g of 2-fluoro-6-octyloxy3-(4-octyloxyphenyl)pyridine. ##STR23##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05630962
Quelldatensatzuspto-grants-1997_05
ORD IDord-dbb292851d0f40bdbc3c5e9e4eedc4a7
Quellennotizuspto-grants-1997_05