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

HRID 1878044
ノート
印刷プレビュー

反応式

HRID 1878044 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

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%.

後処理

  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%

出典と根拠

ORDレコード
ord-a63ae8437b9249b89b48a4ddf0d7b42d
出典データセット
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08314101B2

反応ノート

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