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

HRID 630115
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HRID 630115 반응식
[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]
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참가 물질

5

반응물 3

HCID 962WaterHCID 6340IodoethaneHCID 27958874-methyl-1H-imidazole-5-carbaldehyde

생성물 1

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

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

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).

후처리

  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)

출처 및 근거

ORD 기록
ord-c62358bd86e34960842cc448a873fb72
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09315521B2

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