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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 864264Erstellt: 25. Oktober 2026

Ethanol → 2-Fluoro-6-(4-octyloxyphenyl)pyrazine

https://huagongshe.com/reaction/864264

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktSodium CarbonateHCID 10340—
Edukt4-n-Octyloxyphenylboronic Acid (contains varying amounts of Anhydride)HCID 3977284—
Edukt2-Chloro-6-fluoropyrazineHCID 23273378—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelBenzeneHCID 241—
LösungsmittelWaterHCID 962—
Produkt2-Fluoro-6-(4-octyloxyphenyl)pyrazineHCID 2180463494,7%

Reaktionsschritte

7.99 g (60.0 mmol) of 2-chloro-6-fluoropyrazine, 15.08 g (60.0 mmol) of 4-octyloxyphenylboronic acid, 12.78 g (120.0 mmol) of sodium carbonate and 0.72 g (0.6 mmol) of tetrakis(triphenylphosphine)palladium(0) are heated at 80° C. for 2 hours in 400 ml of benzene, 300 ml of ethanol and 150 ml of water. The reaction mixture is partitioned between aqueous sodium chloride solution and ether, the organic phase is washed with aqueous sodium chloride solution, dried over sodium sulfate, filtered and freed from the solvents, and the residue is purified by chromatography (silica gel/hexane: ethyl acetate = 8:2). 17.18 g of 2-fluoro-6-(4-octyloxyphenyl)pyrazine are obtained. ##STR15## 1c

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05562859
Quelldatensatzuspto-grants-1996_10
ORD IDord-6998e2e71ad14421b508456399b3d2bd
Quellennotizuspto-grants-1996_10