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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1873405Erstellt: 27. Oktober 2026

Water → 2-(4-Propylphenyl)selenophene

https://huagongshe.com/reaction/1873405

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium CarbonateHCID 10340—
Edukt2-BromoselenopheneHCID 137013—
Edukt(4-Propylphenyl)boronic acidHCID 4100861—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelToluene ethanolHCID 21863594—
Produkt2-(4-Propylphenyl)selenopheneHCID 59456318—

Reaktionsschritte

A mixture of 26.0 g (0.12 mol) of 2-bromoselenophene, 20.5 g (0.13 mol) of 4-propylphenylboronic acid, 7.0 g (6.1 mmol) of tetrakis-(triphenylphosphine)palladium(0) and 140 ml of 2 N sodium carbonate soln. in 300 ml of toluene/ethanol (1:1) is heated under reflux for 20 h. A further 7.0 g (6.06 mmol) of tetrakis(triphenylphosphine)palladium(0) are added, and the mixture is refluxed again for 3 h. After cooling, water is added, and the organic phase is separated off. The aqueous phase is extracted with toluene, and the combined organic phases are washed with water 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). 2-(4-Propylphenyl)selenophene is obtained as a yellow liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08304036B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-a75389601c804176925a13fc513e3467
Quellennotizuspto-grants-2012_11