ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

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

HRID 374660
ノート
印刷プレビュー

反応式

HRID 374660 の反応式
[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]
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-benzoquinoneHCID 189969618-Fluoro-2-formyl-5-methoxytetralone

生成物 1

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

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-1f37db10a2404eab8bd068a2dea3068e
出典データセット
uspto-grants-1996_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05480873

反応ノート

読み込み中…

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