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2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 1-Hydroxy-5-methoxy-8-fluoro-2-naphthaldehyde

HRID 374660
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HRID 374660 반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:15][CH3:16])=[C:6]2[C:11]=1[C:10](=[O:12])[CH:9]([CH:13]=[O:14])[CH2:8][CH2:7]2.ClC1C(=O)C(C#N)=C(C#N)C(=O)C=1Cl>O1CCOCC1>[OH:12][C:10]1[C:11]2[C:6](=[C:5]([O:15][CH3:16])[CH:4]=[CH:3][C:2]=2[F:1])[CH:7]=[CH:8][C:9]=1[CH:13]=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 67752,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 189969618-Fluoro-2-formyl-5-methoxytetralone

생성물 1

HCID 104434321-Hydroxy-5-methoxy-8-fluoro-2-naphthaldehyde

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

8-Fluoro-2-formyl-5-methoxy-1-tetralone (20 g) was dissolved in dioxan. 2,3-Dichloro-5,6-dicyanobenzoquinone (21 g) was added and the mixture was heated under reflux for 2 hours. The mixture was allowed to cool and was filtered to remove solids. The solvent was removed under reduced pressure and the residue taken up in ethyl acetate. The product solution was washed with saturated NaHCO3 (aq) (×3), dried (MgSO4), filtered and evaporated to give a dark solid. This material was recrystallised from ethyl acetate/hexane to give 1-hydroxy-5-methoxy-8-fluoro-2-naphthaldehyde, m.p. 156°-158° C.

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 2 hours
  3. temperatureto cool
  4. filtrationwas filtered
  5. customto remove solids
  6. customThe solvent was removed under reduced pressure
  7. washThe product solution was washed with saturated NaHCO3 (aq) (×3)
  8. dry with materialdried (MgSO4)
  9. filtrationfiltered
  10. customevaporated
  11. customto give a dark solid
  12. customThis material was recrystallised from ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-1f37db10a2404eab8bd068a2dea3068e
출처 데이터셋
uspto-grants-1996_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05480873

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