참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | 2-Butyl-5-chloro-3-(4-nitro-benzyl)-3h-imidazole-4-carbaldehyde | HCID 19815397 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 촉매 | Benzyltriphenylphosphonium chloride | HCID 70671 | — |
| 생성물 | 1-(4-Nitrobenzyl)-2-butyl-4-chloro-5-(2-phenylethen-1-yl)imidazole | HCID 54113661 | — |
반응 단계
A solution of 0.4 g of benzyltriphenylphosphonium chloride in 20 ml of dried THF was cooled to -30°. To the above solution was added 0.65 mL of 1.6 M n-BuLi dropwise. As the BuLi was added the solution turned to deep orange color. After stirring for 10 min. at -30°, 0.32 g of 1-(4-nitrobenzyl)-2-butyl-4-chloroimidazole-5-aldehyde was added and the reaction mixture was allowed to warm up to room temperature and stirred at room temperature for 2 hours. The reaction mixture was quenched with 2 mL of saturated NH4Cl solution and diluted with ethyl acetate, and the ethyl acetate solution was washed with water and a brine solution. Evaporation gave a thick oil residue which was purified by the flash silica gel column chromatography (hexane:ethyl acetate=3:1 elution) to give a thick yellow oil, 0.39 g.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05128355 |
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| 출처 데이터셋 | uspto-grants-1992_07 |
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| ORD ID | ord-0e9fa32cf7744476a03699f607183bfc |
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| 출처 메모 | uspto-grants-1992_07 |
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