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Water → 1-ethyl-4-methyl-1H-imidazole-5-carbaldehyde

HRID 577073
ノート
印刷プレビュー

反応式

HRID 577073 の反応式
[CH3:1][C:2]1[N:3]=[CH:4][NH:5][C:6]=1[CH:7]=[O:8].I[CH2:10][CH3:11].O>C1COCC1>[CH2:10]([N:5]1[C:6]([CH:7]=[O:8])=[C:2]([CH3:1])[N:3]=[CH:4]1)[CH3:11]
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 962WaterHCID 6340IodoethaneHCID 27958874-methyl-1H-imidazole-5-carbaldehyde

生成物 1

HCID 595894631-ethyl-4-methyl-1H-imidazole-5-carbaldehyde収率 13%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To 4-methyl-1H-imidazole-5-carbaldehyde (5.0 g, 45.4 mmol) in anhydrous THF (50 mL) was added diaza(1,3)bicyclo[5.4.0]undecane (DBU, 6.8 mL, 45.4 mmol), and iodoethane (3.4 mL, 45.4 mmol). The mixture was stirred at room temperature overnight. Water (50 mL) was added before the THF was evaporated. The mixture was extracted with EtOAc (1×50 mL) and 2-butanol (2×50 mL). The organic extracts were combined, dried over MgSO4, filtered, evaporated, and dried in vacuo. The crude product was purified by flash chromatography (0-1% MeOH/DCM), affording 1-ethyl-4-methyl-1H-imidazole-5-carbaldehyde (806 mg, 13% yield).

後処理

  1. customwas evaporated
  2. extractionThe mixture was extracted with EtOAc (1×50 mL) and 2-butanol (2×50 mL)
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. customevaporated
  6. customdried in vacuo
  7. customThe crude product was purified by flash chromatography (0-1% MeOH/DCM)

出典と根拠

ORDレコード
ord-363faa943eac47d9b6f27cce2d43d3dd
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09040538B2

反応ノート

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