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O-Phenylenediamine → 2-(4-Bromophenyl)-3-phenylquinoxaline

HRID 1878044
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HRID 1878044 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=O)[C:9]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=O)=[CH:4][CH:3]=1.[C:18]1([NH2:25])[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[NH2:24]>C(O)C>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)=[N:25][C:18]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[N:24]=2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7243O-PhenylenediamineHCID 2367011-(4-Bromophenyl)-2-phenylethane-1,2-dione

생성물 1

HCID 18497902-(4-Bromophenyl)-3-phenylquinoxaline

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

In a 200 mL recovery flask were placed 4.5 g (15 mmol) of 1-(4-bromophenyl)-2-phenylethanedione, 1.8 g (17 mmol) of ortho-phenylenediamine, and 50 mL of ethanol. This solution was refluxed under nitrogen stream for 2.5 hours. After a predetermined time, the solution was cooled to room temperature, and the precipitated solid was collected by suction filtration. The collected solid was washed with ethanol; thus, 5.2 g of target white powder was obtained with a yield of 92%.

후처리

  1. customIn a 200 mL recovery flask were placed
  2. temperatureThis solution was refluxed under nitrogen stream for 2.5 hours
  3. filtrationthe precipitated solid was collected by suction filtration
  4. washThe collected solid was washed with ethanol
  5. customthus, 5.2 g of target white powder was obtained with a yield of 92%

출처 및 근거

ORD 기록
ord-a63ae8437b9249b89b48a4ddf0d7b42d
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08314101B2

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