Hexane → 2-(3-Fluorophenyl)-dibenzo[f,h]quinoxaline

HRID 1253385

반응식

HRID 1253385 반응식
CCCCCC.C([Li])CCC.Br[C:13]1[CH:14]=[C:15]([F:19])[CH:16]=[CH:17][CH:18]=1.[N:20]1[C:29]2[C:24](=[C:25]3[CH:37]=[CH:36][CH:35]=[CH:34][C:26]3=[C:27]3[CH:33]=[CH:32][CH:31]=[CH:30][C:28]3=2)[N:23]=[CH:22][CH:21]=1>ClCCl.O.O1CCCC1>[F:19][C:15]1[CH:14]=[C:13]([C:22]2[CH:21]=[N:20][C:29]3[C:24](=[C:25]4[CH:37]=[CH:36][CH:35]=[CH:34][C:26]4=[C:27]4[CH:33]=[CH:32][CH:31]=[CH:30][C:28]4=3)[N:23]=2)[CH:18]=[CH:17][CH:16]=1

참가 물질

8

반응물 4

HCID 8058HexaneHCID 140821-Bromo-3-fluorobenzeneHCID 252644Dibenzo(f,h)quinoxalineHCID 178418339Butyllithium

생성물 1

HCID 577301122-(3-Fluorophenyl)-dibenzo[f,h]quinoxaline수율 23%

시약·촉매·용매 3

HCID 962Water용매HCID 6344Dichloromethane용매HCID 8028Tetrahydrofuran용매

반응 조건

온도
-78 °C

실험 절차

First, under a nitrogen atmosphere, 27.5 mL (1.58 mol/L) of a hexane solution of n-butyllithium was dripped into a mixed solution of 6.87 g of 3-bromofluorobenzene and 40 mL of tetrahydrofuran at −78° C. Then, with the temperature maintained at −78° C., the mixture was stirred for 2 hours. To the obtained solution was added 7.54 g of dibenzo[f,h]quinoxaline in five additions at −78° C. The mixture was heated to room temperature,and stirred for 12 hours with the temperature maintained at room temperature. Water was added to this mixture and dichloromethane was used as an extraction solvent, so that an organic layer was extracted. The obtained organic layer was dried with anhydrous magnesium sulfate. The solution obtained by the drying was filtrated. The solvent of this solution was distilled off, and then, by recrystallization with ethanol, the organometallic complex of the present invention, Hdbq-3FP, which was the target substance, was obtained (a light-orange powder, yield: 23%). Synthesis scheme of Step 1 is shown in (a-2) below.

후처리

  1. temperatureThe mixture was heated to room temperature
  2. stirringstirred for 12 hours with the temperature
  3. temperaturemaintained at room temperature
  4. extractionwas extracted
  5. dry with materialThe obtained organic layer was dried with anhydrous magnesium sulfate
  6. customThe solution obtained by the drying
  7. filtrationwas filtrated
  8. distillationThe solvent of this solution was distilled off
  9. customby recrystallization with ethanol
  10. customwas obtained (a light-orange powder, yield: 23%)
  11. customSynthesis scheme of Step 1

출처 및 근거

ORD 기록
ord-9ce8d8eff8144a85b70142db6700de48
출처 데이터셋
uspto-grants-2013_06
특허 번호
US08455111B2

연결된 노트

불러오는 중…