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Aluminum(III) Chloride → 4-Chloro-7-hydroxycinnoline

HRID 7506
ノート
印刷プレビュー

反応式

HRID 7506 の反応式
[Cl-].[Cl-].[Cl-].[Al+3].[Cl:5][C:6]1[C:15]2[C:10](=[CH:11][C:12]([O:16]C)=[CH:13][CH:14]=2)[N:9]=[N:8][CH:7]=1>C1C=CC=CC=1>[Cl:5][C:6]1[C:15]2[C:10](=[CH:11][C:12]([OH:16])=[CH:13][CH:14]=2)[N:9]=[N: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 6451240Aluminum(III) ChlorideHCID 219910214-Chloro-7-methoxycinnoline

生成物 1

HCID 1360879794-Chloro-7-hydroxycinnoline収率 53.6%

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

Aluminium trichloride (2.6 g, 19 mmol) was added in portions to a suspension of 4-chloro-7-methoxycinnoline (0.9 g, 3.8 mmol), (J. Chem. Soc. 1955, 2100), in benzene (15 ml) and the mixture was heated at reflux for 1 hour. The solvent was removed by evaporation and the residue was partitioned between ice/water and ethyl acetate. Aqueous saturated sodium chloride solution was added and the organic layer was separated. The organic layer was washed with brine, dried (MgSO4) and the solvent removed by evaporation. The residue was triturated with ether, collected, filtered and dried under vacuum to give 4-chloro-7-hydroxycinnoline (368 mg, 53%).

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

後処理

  1. temperaturethe mixture was heated
  2. temperatureat reflux for 1 hour
  3. customThe solvent was removed by evaporation
  4. customthe residue was partitioned between ice/water and ethyl acetate
  5. additionAqueous saturated sodium chloride solution was added
  6. customthe organic layer was separated
  7. washThe organic layer was washed with brine
  8. dry with materialdried (MgSO4)
  9. customthe solvent removed by evaporation
  10. customThe residue was triturated with ether
  11. customcollected
  12. filtrationfiltered
  13. customdried under vacuum

出典と根拠

ORDレコード
ord-40bee509c4af45dea8ed128cbd63add2
出典データセット
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07087602B2

反応ノート

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