참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Allyl bromide | HCID 7841 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-Methylbenzoyl Chloride | HCID 13405 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 반응물 | HCID 178418822 | HCID 178418822 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (1-Allyl-4-phenyl-1H-imidazole-2-yl)(4-methylphenyl)methanone | HCID 59863324 | 30% |
반응 단계
Potassium t-butoxide (2.59 g, 23.1 mmol) was dissolved in DMF (100 ml), and thereto was added 4-phenyl-1H-imidazole (3.00 g, 21 mmol) with stirring. The mixture was stirred at room temperature for 30 minutes, and thereto was added allyl bromide (3.50 g, 31.5 mmol). The mixture was stirred at 40° C. for 4 hours. To the reaction solution was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated saline, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The resulting residue was dissolved in pyridine (24 ml), and thereto were added successively triethylamine (17.9 g, 17.7 mmol) and 4-toluoyl chloride (3.7 g, 16.3 mmol), and the mixture was stirred at 60° C. for 5 hours. To the reaction solution was added water (50 ml), and the mixture was extracted with ethyl acetate. The organic layer was washed with water, 1N diluted hydrochloric acid, and saturated saline, and dried over magnesium sulfate. Then, the solvent was evaporated under reduced pressure, and the resulting residue was purified by silica gel column chromatography to give the title compound (760 mg, 30%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07425642B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-bf2eefba035149b195bd8b452f9e4bb0 |
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| 출처 메모 | uspto-grants-2008_09 |
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