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2-Methylimidazole → 4-(2-Methyl-1H-imidazol-1-yl)benzaldehyde

HRID 1291044
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HRID 1291044 반응식
[H-].[Na+].[CH3:3][C:4]1[NH:5][CH:6]=[CH:7][N:8]=1.F[C:10]1[CH:17]=[CH:16][C:13]([CH:14]=[O:15])=[CH:12][CH:11]=1>CN(C=O)C>[CH3:3][C:4]1[N:5]([C:10]2[CH:17]=[CH:16][C:13]([CH:14]=[O:15])=[CH:12][CH:11]=2)[CH:6]=[CH:7][N:8]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 127492-MethylimidazoleHCID 24758Sodium hydrideHCID 680234-Fluorobenzaldehyde

생성물 1

HCID 31596624-(2-Methyl-1H-imidazol-1-yl)benzaldehyde수율 35.8%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

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온도
10 °C

실험 절차

To a suspension of NaH (0.612 g, 15.3 mmol : 60% suspension of mineral oil) of in dry DMF (10 ml) cooled to 10° C. was added a DMF (8 ml) solution of 2-methylimidazole (1.23 g, 15 mmol) under a nitrogen atmosphere, and the mixture was stirred for 30 min at room temperature. 4-Fluorobenzaldehyde (1.90 g, 15.3 mmol) was added to the reaction mixture, and the resulting solution was stirred for 14 h. The reaction mixture was poured into an ice-cold saturated aqueous NH4Cl solution (100 ml) and extracted with ethyl acetate (100 ml×2). The organic layer was washed with water (100 ml) and brine (80 ml), dried over MgSO4 and the solvent removed under reduced pressure. The resultant residue was purified by column chromatography (SiO2 ; hexane:ethyl acetate=1:1 then ethyl acetate) to give crude 4-(2-methylimidazol-1-yl)-benzaldehyde (1.0 g), which was used without further purification.

후처리

  1. stirringthe resulting solution was stirred for 14 h
  2. extractionextracted with ethyl acetate (100 ml×2)
  3. washThe organic layer was washed with water (100 ml) and brine (80 ml)
  4. dry with materialdried over MgSO4
  5. customthe solvent removed under reduced pressure
  6. customThe resultant residue was purified by column chromatography (SiO2

출처 및 근거

ORD 기록
ord-083e4b7aaf344ee7a67681396c9378a1
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05753682

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