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Imidazole → 4[3-(1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehyde

HRID 485799
ノート
印刷プレビュー

反応式

HRID 485799 の反応式
[NH:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.[H-].[Na+].Br[CH2:9][CH2:10][CH2:11][CH:12]1[CH2:17][CH2:16][N:15]([CH:18]=[O:19])[CH2:14][CH2:13]1>CN(C)C=O>[N:1]1([CH2:9][CH2:10][CH2:11][CH:12]2[CH2:13][CH2:14][N:15]([CH:18]=[O:19])[CH2:16][CH2:17]2)[CH:5]=[CH:4][N:3]=[CH:2]1
参加物反応条件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 795ImidazoleHCID 24758Sodium hydrideHCID 202397684-(3-Bromopropyl)-1-piperidinecarboxaldehyde

生成物 1

HCID 137267384[3-(1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehyde収率 96%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

反応条件

温度
50 °C

実験手順

The mixture of imidazole (0.7 g, 0.01M) and NaH (50% by weight in mineral oil, 0.9 g, 0.018M) in dimethylformamide (60 ml) was heated at 50° C. for 1/2 hr. and 4-(3-bromopropyl)-1-piperidinecarboxaldehyde (2.93 g, 0.0125M) in dimethylformamide (20 ml) was added. The reaction was heated at 50° C. for 4 hrs. After the reaction, the solvent was removed in vacuo, water was added and the product was extracted with CH2Cl2 (3×50 ml). The combined extracts, dried over Na2SO4, were stripped to dryness and purified on silica gel column eluted with 10% by volume methanol--90% by volume methylenechloride to give 4[3-(1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehyde as an oil (2.12 g, 96%).

後処理

  1. temperatureThe reaction was heated at 50° C. for 4 hrs
  2. customAfter the reaction
  3. customthe solvent was removed in vacuo, water
  4. additionwas added
  5. extractionthe product was extracted with CH2Cl2 (3×50 ml)
  6. dry with materialThe combined extracts, dried over Na2SO4
  7. custompurified on silica gel column
  8. washeluted with 10% by volume methanol--90% by volume methylenechloride

出典と根拠

ORDレコード
ord-1f910d0d65774e6ba7661bac113d5eb4
出典データセット
uspto-grants-1985_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04537969

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート