참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phenethyl bromide | HCID 7666 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 1H-Imidazole-4-carbaldehyde | HCID 76428 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-Phenethyl-1H-imidazole-4-carbaldehyde | HCID 22289872 | — |
반응 단계
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+].
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06713496B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-31441750fe72498fa9d8520b043eb1a1 |
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| 출처 메모 | uspto-grants-2004_03 |
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