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HRID 553373作成日:2026年10月26日

Hexane → Quinoxaline

https://huagongshe.com/reaction/553373

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物1-Bromo-3-fluorobenzeneHCID 14082—
反応物Dibenzo(f,h)quinoxalineHCID 252644—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物QuinoxalineHCID 704523%

反応条件

温度-78 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08048540B2
出典データセットuspto-grants-2011_11
ORD IDord-1617ea16548341dda3c0b7cbbb9ed5e4
出典メモuspto-grants-2011_11