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2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 5-Bromoacenaphthylene

HRID 919179
ノート
印刷プレビュー

反応式

HRID 919179 の反応式
[Br:1][C:2]1[C:12]2[C:13]3[C:5]([CH2:6][CH2:7][C:8]=3[CH:9]=[CH:10][CH:11]=2)=[CH:4][CH:3]=1.ClC1C(=O)C(C#N)=C(C#N)C(=O)C=1Cl>C1C=CC=CC=1>[Br:1][C:2]1[C:12]2[C:13]3[C:5]([CH:6]=[CH:7][C:8]=3[CH:9]=[CH:10][CH:11]=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 67752,3-Dichloro-5,6-dicyano-1,4-benzoquinone2 回HCID 749235-Bromoacenaphthene

生成物 1

HCID 122444035-Bromoacenaphthylene収率 52.4%

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

To 25.4 g (107.3 mmol) of 5-bromoacenaphthene and 500 mL of dehydrated benzene, 29.2 g (128.7 mmol) of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) was added, and the mixture was stirred for 6 hours under heat refluxing. Furthermore, 6.0 g (26.4 mmol) of DDQ was added to the reaction mixture, and the mixture was stirred for 4 hours by heating. After allowing the resultant mixture to stand for cooling, a precipitate was filtered off and washed with chloroform. Filtrates were combined and washed with a 10% sodium hydroxide aqueous solution and water. After liquid separation, an organic phase was dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was dried under reduced pressure to obtain 13.0 g (yield: 51.6%) of 5-bromoacenaphthylene as a brown solid.

後処理

  1. temperatureunder heat
  2. temperaturerefluxing
  3. stirringthe mixture was stirred for 4 hours
  4. temperatureby heating
  5. temperaturefor cooling
  6. filtrationa precipitate was filtered off
  7. washwashed with chloroform
  8. washwashed with a 10% sodium hydroxide aqueous solution and water
  9. customAfter liquid separation
  10. dry with materialan organic phase was dried over anhydrous sodium sulfate
  11. distillationthe solvent was distilled off
  12. customThe residue was dried under reduced pressure

出典と根拠

ORDレコード
ord-f75f00d9d44545a295959e70f55cb421
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09273002B2

反応ノート

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