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Bromine → 5-Bromo-4-propylpyridine-2-amine

HRID 1038546
ノート
印刷プレビュー

反応式

HRID 1038546 の反応式
[CH2:1]([C:4]1[CH:9]=[CH:8][N:7]=[C:6]([NH2:10])[CH:5]=1)[CH2:2][CH3:3].[Br:11]Br.C(=O)([O-])O.[Na+]>C(O)C>[Br:11][C:9]1[C:4]([CH2:1][CH2:2][CH3:3])=[CH:5][C:6]([NH2:10])=[N:7][CH:8]=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 24408BromineHCID 516892Sodium BicarbonateHCID 70225944-Propylpyridin-2-amine

生成物 1

HCID 665984465-Bromo-4-propylpyridine-2-amine収率 48%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

実験手順

To a solution of 4-propylpyridin-2-amine (5.70 g, 41.8 mmol) in ethanol (210 mL), a solution of bromine in ethanol (bromine 2.38 mL/ethanol 50 mL) was added under ice-cold conditions, and the mixture was stirred under ice-cold conditions for 0.5 hours. Under ice-cold conditions, the reaction solution was added an aqueous solution of sodium hydrogen carbonate, concentrated in vacuo, and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The obtained residue was purified by silica-gel column chromatography (hexane/ethyl acetate), and the title compound (4.34 g (yield 48%)) was obtained as a brown oil.

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. concentrationconcentrated in vacuo
  2. extractionextracted with ethyl acetate
  3. washThe organic layer was washed with brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated in vacuo
  6. customThe obtained residue was purified by silica-gel column chromatography (hexane/ethyl acetate)

出典と根拠

ORDレコード
ord-4b474b17b47a42eb9175d6def1badd3e
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08551985B2

反応ノート

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