تفاعل #640555
ord-1617ea16548341dda3c0b7cbbb9ed5e4
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىseparate additions
- 2درجة الحرارةThe reaction temperature was increased to room temperature
- 3workup.STIRRINGthe solution was stirred at room temperature for 12 hours
- 4workup.ADDITIONWater was added to this mixture
- 5استخلاصan organic layer was extracted with dichloromethane
- 6تجفيفThe obtained organic layer was dried over anhydrous magnesium sulfate
- 7ترشيحThe dried solution was filtered
- 8workup.DISTILLATIONAfter the solvent of this solution was distilled
- 9أخرىthe resultant substance was recrystallized with ethanol
الإجراء التجريبي
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).