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1-Iodopropane → HCID 22494700、化合物

HRID 1816706
ノート
印刷プレビュー

反応式

HRID 1816706 の反応式
[C:1]([S:4][CH:5]1[CH2:10][CH2:9][N:8]([C:11]2[CH:16]=[CH:15][C:14]([N+:17]([O-])=O)=[CH:13][CH:12]=2)[CH2:7][CH2:6]1)(=O)[CH3:2].CO.C[O-].[Na+].I[CH2:26]CC>C1COCC1.CO>[CH2:1]([S:4][CH:5]1[CH2:10][CH2:9][N:8]([C:11]2[CH:16]=[CH:15][C:14]([NH2:17])=[CH:13][CH:12]=2)[CH2:7][CH2:6]1)[CH2:2][CH3:26]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 336431-IodopropaneHCID 22494742HCID 22494742、化合物HCID 23694274Sodium methanolate methanol

生成物 1

HCID 22494700HCID 22494700、化合物

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 4-(4-acetylthiopiperidin-1-yl)nitrobenzene (3.34 g) in a mixture of THF (30 ml) and methanol (30 ml) was added 28% sodium methoxide methanol solution (2.67 ml) at 0-5° C. and stirred at the same temperature for 30 minutes. To the mixture was added iodopropane (1.51 ml) at the same temperature and stirred at ambient temperature for 2 hours. The reaction mixture was evaporated in vacuo and dissolved in ethyl acetate (100 ml). The solution was washed three times with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo. A solution of the resulting residue, ammonium chloride (1.0 g) and iron powder (4.0 g) in a mixture of ethanol (60 ml) and water (30 ml) was refluxed for 2 hours. The reaction mixture was evaporated in vacuo. The resulting residue was chromatographed on silica gel (300 ml) eluting with ethyl acetate. The fractions containing the desired compound were collected and evaporated under reduced pressure to give 4-(4-propylthiopiperidin-1-yl)aniline (2.47 g).

後処理

  1. stirringstirred at ambient temperature for 2 hours
  2. customThe reaction mixture was evaporated in vacuo
  3. dissolutiondissolved in ethyl acetate (100 ml)
  4. washThe solution was washed three times with saturated aqueous sodium chloride
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customevaporated in vacuo
  7. additionA solution of the resulting residue, ammonium chloride (1.0 g) and iron powder (4.0 g) in a mixture of ethanol (60 ml) and water (30 ml)
  8. temperaturewas refluxed for 2 hours
  9. customThe reaction mixture was evaporated in vacuo
  10. customThe resulting residue was chromatographed on silica gel (300 ml)
  11. washeluting with ethyl acetate
  12. additionThe fractions containing the desired compound
  13. customwere collected
  14. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-7fb24c90683a4fa39a1b04eb8d3fb660
出典データセット
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06884868B1

反応ノート

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