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Selenium Dioxide → 7-(2-Methoxyethoxy)-8-methylquinoline-2-carbaldehyde

HRID 338923
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HRID 338923 반응식
[CH3:1][O:2][CH2:3][CH2:4][O:5][C:6]1[C:15]([CH3:16])=[C:14]2[C:9]([CH:10]=[CH:11][C:12]([CH3:17])=[N:13]2)=[CH:8][CH:7]=1.[Se](=O)=[O:19]>O1CCOCC1.O>[CH3:1][O:2][CH2:3][CH2:4][O:5][C:6]1[C:15]([CH3:16])=[C:14]2[C:9]([CH:10]=[CH:11][C:12]([CH:17]=[O:19])=[N:13]2)=[CH:8][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24007Selenium DioxideHCID 709840567-(2-Methoxyethoxy)-2,8-dimethylquinoline

생성물 1

HCID 867074527-(2-Methoxyethoxy)-8-methylquinoline-2-carbaldehyde수율 70%

시약·촉매·용매 1

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

실험 절차

To 7-(2-methoxyethoxy)-2,8-dimethylquinoline (90 mg, 0.39 mmol) in dioxane/water (5 mL/0.5 mL) at ambient temperature was added selenium dioxide (52 mg, 0.47 mmol) and the reaction was heated to reflux for 1 hour. After cooling, the reaction was filtered and the solids washed with DCM. The filtrate was dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by reverse phase chromatography (SP4, 12M, eluting with a gradient of water/ACN 100:0 to 0:100, 20 column volumes) to yield 7-(2-methoxyethoxy)-8-methylquinoline-2-carbaldehyde (67 mg, 70% yield) as a tan solid.

후처리

  1. temperaturethe reaction was heated
  2. temperatureto reflux for 1 hour
  3. temperatureAfter cooling
  4. filtrationthe reaction was filtered
  5. washthe solids 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, 12M
  10. washeluting with a gradient of water/ACN 100:0 to 0:100, 20 column volumes)

출처 및 근거

ORD 기록
ord-336d486b403c45b0b68eef6e3a4c5de1
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08889704B2

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