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Sodium Methoxide → 7-Fluoro-2-methoxy-8-methylquinoxaline

HRID 2233167
ノート
印刷プレビュー

反応式

HRID 2233167 の反応式
Cl[C:2]1[CH:11]=[N:10][C:9]2[C:4](=[C:5]([CH3:13])[C:6]([F:12])=[CH:7][CH:8]=2)[N:3]=1.[CH3:14][O-:15].[Na+]>CO>[F:12][C:6]1[C:5]([CH3:13])=[C:4]2[C:9]([N:10]=[CH:11][C:2]([O:15][CH3:14])=[N:3]2)=[CH:8][CH:7]=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 10942334Sodium MethoxideHCID 866283592-Chloro-7-fluoro-8-methylquinoxaline

生成物 1

HCID 675481507-Fluoro-2-methoxy-8-methylquinoxaline収率 96%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

2-Chloro-7-fluoro-8-methylquinoxaline (4.1 g, 20.9 mmol) was suspended in dry methanol and a 25% solution of sodium methoxide in methanol (4.73 ml, 21.9 mmol) was added by syringe. The mixture was heated under reflux for 2 h, then evaporated. The residue was dissolved in dichloromethane and water and the phases were separated. The aqueous phase was extracted twice with dichloromethane, and combined organic fractions were dried and evaporated to give product (3.84 g, 96%).

後処理

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 2 h
  3. customevaporated
  4. dissolutionThe residue was dissolved in dichloromethane
  5. customwater and the phases were separated
  6. extractionThe aqueous phase was extracted twice with dichloromethane
  7. customwere dried
  8. customevaporated

出典と根拠

ORDレコード
ord-a142b70347a1436ba085ad7f7903088e
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07709483B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート