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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 553373Erstellt: 24. Oktober 2026

Hexane → Quinoxaline

https://huagongshe.com/de/reaction/553373

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
Edukt1-Bromo-3-fluorobenzeneHCID 14082—
EduktDibenzo(f,h)quinoxalineHCID 252644—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktQuinoxalineHCID 704523%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

First, 27.5 mL of a hexane solution of n-butyllithium (1.58 mol/L) was dropped in a mixed solution of 6.87 g of 3-bromofluorobenzene and 40 mL of tetrahydrofuran at −78° C. under nitrogen atmosphere, and immediately after that, the obtained solution was stirred at −78° C. for 2 hours. To this solution was added 7.54 g of dibenzo[f,h]quinoxaline at −78° C. in five separate additions. The reaction temperature was increased to room temperature, and then the solution was stirred at room temperature for 12 hours. Water was added to this mixture, and an organic layer was extracted with dichloromethane used as an extraction solvent. The obtained organic layer was dried over anhydrous magnesium sulfate. The dried solution was filtered. After the solvent of this solution was distilled, the resultant substance was recrystallized with ethanol to obtain an objective quinoxaline derivative Hdbq-3FP (light orange power, yield 23%). Synthetic scheme of Step 1 is shown in the following (a-2).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08048540B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-1617ea16548341dda3c0b7cbbb9ed5e4
Quellennotizuspto-grants-2011_11