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5-Nitroindole → HCID 21202645、化合物

HRID 1978921
ノート
印刷プレビュー

反応式

HRID 1978921 の反応式
[N+:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[NH:9][CH:8]=[CH:7]2)([O-:3])=[O:2].[H-].[Na+].[CH3:15][O:16][C:17](=[O:23])[CH2:18][CH2:19][CH2:20][CH2:21]Br>C(#N)C>[CH3:15][O:16][C:17]([CH2:18][CH2:19][CH2:20][CH2:21][N:9]1[C:10]2[C:6](=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:12][CH:11]=2)[CH:7]=[CH:8]1)=[O:23]
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 225235-NitroindoleHCID 24758Sodium hydrideHCID 79557Methyl 5-bromovalerate

生成物 1

HCID 21202645HCID 21202645、化合物収率 91%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒2 回

実験手順

To a stirred solution of 5-nitroindole (0.324 g, 2.0 mmol) in anhydrous acetonitrile (10 ml) was added sodium hydride (0.057 g, 2.38 mmol). The resulting red-brown solution was stirred for 45 minutes, before the addition of a solution of methyl-5-bromovalerate (0.429 g, 2.2 mmol) in anhydrous acetonitrile (1 ml). The solution was stirred for 21 hours, during which time a solid precipitated. Analysis by TLC in chloroform:ethanol (99:1) after 2 hours showed 2 components (starting material: Rf=0.5, 1-(4-methoxycarbonyl butyl)5-nitroindole: Rf=0.8). Further analysis after 21 hours indicated the reaction was essentially complete. The reaction mixture was poured into ethyl acetate (20 ml) and molar HCl (20 ml) and the phases separated. The aqueous phase was extracted with ethyl acetate (20 ml) and the combined organic layer washed with molar sodium bicarbonate solution. The ethyl acetate solution was dried over anhydrous sodium sulphate, filtered and rotary evaporated to give a yellow oil (0.5 g, 1.81 mmol, 91%).

後処理

  1. customprecipitated
  2. waitAnalysis by TLC in chloroform:ethanol (99:1) after 2 hours showed
  3. waitFurther analysis after 21 hours indicated
  4. additionThe reaction mixture was poured into ethyl acetate (20 ml) and molar HCl (20 ml)
  5. customthe phases separated
  6. extractionThe aqueous phase was extracted with ethyl acetate (20 ml)
  7. washthe combined organic layer washed with molar sodium bicarbonate solution
  8. dry with materialThe ethyl acetate solution was dried over anhydrous sodium sulphate
  9. filtrationfiltered
  10. customrotary evaporated

出典と根拠

ORDレコード
ord-2b96bb2ba2654585a2876a387cbf0637
出典データセット
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06239159B1

反応ノート

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