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Ethyl chloroacetate → ethyl (2-formyl-1H-imidazol-1-yl)acetate

HRID 1916376
ノート
印刷プレビュー

反応式

HRID 1916376 の反応式
[NH:1]1[CH:5]=[CH:4][N:3]=[C:2]1[CH:6]=[O:7].CN1CCCC1=O.Cl[CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18].C(=O)([O-])[O-].[K+].[K+]>O>[CH:6]([C:2]1[N:1]([CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18])[CH:5]=[CH:4][N:3]=1)=[O:7]
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 4

HCID 7751Ethyl chloroacetateHCID 11430Potassium CarbonateHCID 13387N-methyl-2-pyrrolidoneHCID 249551H-imidazole-2-carbaldehyde

生成物 1

HCID 62222097ethyl (2-formyl-1H-imidazol-1-yl)acetate

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To 1H-imidazole-2-carboaldehyde (2.0 g), N-methylpyrrolidone (25 mL) was added, followed by dissolution with heating. To the resultant solution, ethyl chloroacetate (11.1 mL) and potassium carbonate (2.9 g) were added. The reaction solution was stirred at room temperature for 14 hours. To the reaction solution, water (30 mL) was added. The aqueous layer was extracted twice with ethyl acetate. The organic layers were combined, washed with saturated saline and then dried over anhydrous sodium sulfate. The anhydrous sodium sulfate was removed by filtration and the solvent was concentrated under reduced pressure. The residue was purified by silica gel chromatography (dichloromethane) to obtain the title compound having the following physical properties (1.3 g).

後処理

  1. dissolutionfollowed by dissolution
  2. temperaturewith heating
  3. extractionThe aqueous layer was extracted twice with ethyl acetate
  4. washwashed with saturated saline
  5. dry with materialdried over anhydrous sodium sulfate
  6. customThe anhydrous sodium sulfate was removed by filtration
  7. concentrationthe solvent was concentrated under reduced pressure
  8. customThe residue was purified by silica gel chromatography (dichloromethane)

出典と根拠

ORDレコード
ord-0565e269818249d3a4ce5913ed66a94e
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08618122B2

反応ノート

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