Hexane → Quinoxaline

HRID 553373

반응식

HRID 553373 반응식
CCCCCC.C([Li])CCC.BrC1C=C(F)C=CC=1.[N:20]1[C:29]2[C:24](=[C:25]3C=CC=C[C:26]3=[C:27]3C=CC=C[C:28]3=2)[N:23]=[CH:22][CH:21]=1>O1CCCC1>[N:20]1[C:29]2[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=2)[N:23]=[CH:22][CH:21]=1

참가 물질

6

반응 조건

온도
-78 °C

실험 절차

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).

후처리

  1. customseparate additions
  2. temperatureThe reaction temperature was increased to room temperature
  3. stirringthe solution was stirred at room temperature for 12 hours
  4. additionWater was added to this mixture
  5. extractionan organic layer was extracted with dichloromethane
  6. dry with materialThe obtained organic layer was dried over anhydrous magnesium sulfate
  7. filtrationThe dried solution was filtered
  8. distillationAfter the solvent of this solution was distilled
  9. customthe resultant substance was recrystallized with ethanol

출처 및 근거

ORD 기록
ord-1617ea16548341dda3c0b7cbbb9ed5e4
출처 데이터셋
uspto-grants-2011_11
특허 번호
US08048540B2

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