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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1873394Erstellt: 26. Oktober 2026

Sodium Carbonate → 2-(4-Ethoxy-2,3-difluorophenyl)selenophene

https://huagongshe.com/reaction/1873394

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt2-BromoselenopheneHCID 137013—
EduktB-(4-Ethoxy-2,3-difluorophenyl)boronic acidHCID 15135235—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelToluene ethanolHCID 21863594—
Produkt2-(4-Ethoxy-2,3-difluorophenyl)selenopheneHCID 59456301—

Reaktionsschritte

A mixture of 45.0 g (0.21 mol) of 2-bromoselenophene, 52.0 g (0.26 mol) of 4-ethoxy-2,3-difluorophenylboronic acid, 20.0 g (17.3 mmol) of tetrakis(triphenylphosphine)palladium(0) and 600 ml of 2 N sodium carbonate soln. in 1100 ml of toluene/ethanol (1:1) is heated under reflux for 20 h. After cooling, the organic phase is separated off, and the aqueous phase is extracted with toluene. The combined organic phases are washed with sat. sodium hydrogencarbonate soln., 1 N hydrochloric acid and sat. sodium chloride soln. The solution is dried using sodium sulfate and concentrated to dryness. The residue is purified by column chromatography (SiO2, n-heptane:toluene=3:2). Further purification is carried out by recrystallisation from ethanol; 2-(4-ethoxy-2,3-difluorophenyl)selenophene is obtained as a beige solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08304036B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-b0d75b2282834822b4ffc49a3ff86c7a
Quellennotizuspto-grants-2012_11