Phenethyl bromide → 1-Phenethyl-1H-imidazole-4-carbaldehyde

HRID 968427

반응식

HRID 968427 반응식
[NH:1]1[CH:5]=[C:4]([CH:6]=[O:7])[N:3]=[CH:2]1.[H-].[Na+].Br[CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>O1CCCC1>[C:13]1([CH2:12][CH2:11][N:1]2[CH:5]=[C:4]([CH:6]=[O:7])[N:3]=[CH:2]2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

참가 물질

5

실험 절차

Imidazole-4-carboxaldehyde (6.73 g, 70 mmol) was added portionwise to a suspension of sodium hydride (1.68 g, 60% dispersion in mineral oil, 70 mmol) in tetrahydrofuran (280 ml), and the mixture was then stirred at room temperature for 30 minutes. (2-Bromoethyl)benzene (9.56 ml, 70 mmol) was added, and the mixture was stirred at room temperature for 72 hours. The mixture was evaporated under reduced pressure and the residue was partitioned between water (300 ml) and dichloromethane (500 ml), and the layers were separated. The organic phase was dried (MgSO4) and evaporated under reduced pressure. The crude product was pre-adsorbed onto silica gel, and purified by column chromatography on silica gel using an elution gradient of ethyl acetate:pentane (50:50 to 100:0) to afford the title compound, 1.44 g. 1H-NMR (CDCl3, 400 MHz) δ: 3.16 (t, 2H), 4.23 (t, 2H), 7.02 (d, 2H), 7.28 (m, 3H), 7.36 (s, 1H), 7.50 (s, 1H), 9.83 (s, 1H). LRMS: m/z (ES+) 223 [MNa+].

후처리

  1. stirringthe mixture was stirred at room temperature for 72 hours
  2. customThe mixture was evaporated under reduced pressure
  3. customthe residue was partitioned between water (300 ml) and dichloromethane (500 ml)
  4. customthe layers were separated
  5. dry with materialThe organic phase was dried (MgSO4)
  6. customevaporated under reduced pressure
  7. custompurified by column chromatography on silica gel using an elution gradient of ethyl acetate:pentane (50:50 to 100:0)

출처 및 근거

ORD 기록
ord-e2df1067444d4e47b08f076064e9aa84
출처 데이터셋
uspto-grants-2005_10
특허 번호
US06958402B2

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