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Sulfuric Acid → 7-Bromo-4-methylquinoline

HRID 1788332
ノート
印刷プレビュー

反応式

HRID 1788332 の反応式
OS(O)(=O)=O.[Br:6][C:7]1[CH:8]=[C:9]([CH:11]=[CH:12][CH:13]=1)[NH2:10].[CH:14]([C:16]([CH3:18])=O)=[CH2:15]>O1CCOCC1>[Br:6][C:7]1[CH:8]=[C:9]2[C:11]([C:16]([CH3:18])=[CH:14][CH:15]=[N:10]2)=[CH:12][CH:13]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 1118Sulfuric AcidHCID 6570Methyl vinyl ketoneHCID 115623-Bromoaniline

生成物 1

HCID 219925517-Bromo-4-methylquinoline

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒2 回

実験手順

H2SO4 (14.4 mL, 270 mmol) is added to a solution of 3-bromoaniline (Aldrich, 30.0 g, 174 mmol) in 1,4-dioxane (1 L) at RT. The mixture is heated to reflux and treated with methyl vinyl ketone (Aldrich, 19.5 mL, 270 mmol) in 1,4-dioxane (50 mL) dropwise over 3 h. Heating is continued for 1 h after the addition, followed by removal of the solvent in vacuo. The residue is dissolved in water (100 mL), neutralized with Na2CO3 and extracted with CH2Cl2. The combined organic extracts are washed with water and brine, dried (Na2SO4) and filtered. The filtrate is concentrated, and the residue chromatographed on silica gel (Biotage, eluting with 20% EtOAc/Hexanes) to give the title compound, 15.0 g (43%), as a brownish solid.

後処理

  1. temperatureThe mixture is heated
  2. temperatureto reflux
  3. temperatureHeating
  4. additionafter the addition
  5. customfollowed by removal of the solvent in vacuo
  6. dissolutionThe residue is dissolved in water (100 mL)
  7. extractionextracted with CH2Cl2
  8. washThe combined organic extracts are washed with water and brine
  9. dry with materialdried (Na2SO4)
  10. filtrationfiltered
  11. concentrationThe filtrate is concentrated
  12. customthe residue chromatographed on silica gel (Biotage, eluting with 20% EtOAc/Hexanes)

出典と根拠

ORDレコード
ord-8f57fa29e9ac49ff89af3b6a105da1ce
出典データセット
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07511065B2

反応ノート

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