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Selenium Dioxide → 6-Fluoro-8-methoxyquinoline-2-carbaldehyde

HRID 338916
ノート
印刷プレビュー

反応式

HRID 338916 の反応式
[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([O:12][CH3:13])[CH:11]=1)[N:8]=[C:7]([CH3:14])[CH:6]=[CH:5]2.[Se](=O)=[O:16]>O1CCOCC1.O>[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([O:12][CH3:13])[CH:11]=1)[N:8]=[C:7]([CH:14]=[O:16])[CH:6]=[CH:5]2
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 24007Selenium DioxideHCID 867074466-Fluoro-8-methoxy-2-methylquinoline

生成物 1

HCID 867074476-Fluoro-8-methoxyquinoline-2-carbaldehyde収率 78.8%

試薬・触媒・溶媒 1

HCID 218864351,4-Dioxane--water (1/1)溶媒

実験手順

To 6-fluoro-8-methoxy-2-methylquinoline (500 mg, 2.62 mmol) in dioxane/water (5 mL/0.5 mL) at ambient temperature was added selenium dioxide (348 mg, 3.14 mmol) and the reaction was heated to reflux for 2-3 hours. After cooling, the reaction was filtered and the solids were washed with DCM. The filtrate was dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by reverse phase chromatography (SP4, 25M, eluting with a gradient of water/ACN 100:0 to 0:100, 20 column volumes) to yield 6-fluoro-8-methoxyquinoline-2-carbaldehyde (423 mg, 78.8% yield) as a tan solid.

後処理

  1. temperaturethe reaction was heated
  2. temperatureto reflux for 2-3 hours
  3. temperatureAfter cooling
  4. filtrationthe reaction was filtered
  5. washthe solids were washed with DCM
  6. dry with materialThe filtrate was dried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified by reverse phase chromatography (SP4, 25M
  10. washeluting with a gradient of water/ACN 100:0 to 0:100, 20 column volumes)

出典と根拠

ORDレコード
ord-8bd726af67dd48d0bf7df369a8ad5013
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08889704B2

反応ノート

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