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Potassium Nitrate → 7-Nitro-1,2,3,4-tetrahydroquinoline

HRID 74037
ノート
印刷プレビュー

反応式

HRID 74037 の反応式
[NH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][CH2:2]1.[N+:11]([O-])([O-:13])=[O:12].[K+].C([O-])(O)=O.[Na+]>OS(O)(=O)=O>[N+:11]([C:8]1[CH:9]=[C:10]2[C:5]([CH2:4][CH2:3][CH2:2][NH:1]2)=[CH:6][CH:7]=1)([O-:13])=[O:12]
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 24434Potassium NitrateHCID 694601,2,3,4-TetrahydroquinolineHCID 516892Sodium Bicarbonate

生成物 1

HCID 2525137-Nitro-1,2,3,4-tetrahydroquinoline収率 25%

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒

実験手順

To a mixture of 1,2,3,4-tetrahydro-quinoline (20.0 g, 0.15 mol) dissolved in H2SO4 (98%, 150 mL), KNO3 (18.2 g, 0.18 mol) was slowly added at 0° C. The reaction was allowed to warm to room temperature and stirred over night. The mixture was then poured into ice-water and basified with sat. NaHCO3 solution to pH 8. After extraction with CH2Cl2, the combined organic layers were washed with brine, dried over Na2SO4 and concentrated. The residue was purified by column chromatography (petroleum ether-EtOAc, 10:1) to give 7-nitro-1,2,3,4-tetrahydro-quinoline (6.6 g, 25%).

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. extractionAfter extraction with CH2Cl2
  2. washthe combined organic layers were washed with brine
  3. dry with materialdried over Na2SO4
  4. concentrationconcentrated
  5. customThe residue was purified by column chromatography (petroleum ether-EtOAc, 10:1)

出典と根拠

ORDレコード
ord-24fffb0f5ed640cfbb893287a6041370
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08829204B2

反応ノート

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