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HRID 563079作成日:2026年10月26日
Dimethylformamide → 4-(4-Chlorophenyl)-5-[3-(2-methylphenoxy)propyl]-2-(2-phenyl-1-imidazolyl)oxazole
https://huagongshe.com/reaction/563079
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 2-Phenylimidazole | HCID 69591 | — |
| 反応物 | 2-Chloro-4-(4-chlorophenyl)-5-[3-(2-methylphenoxy)propyl]oxazole | HCID 10882967 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 4-(4-Chlorophenyl)-5-[3-(2-methylphenoxy)propyl]-2-(2-phenyl-1-imidazolyl)oxazole | HCID 18174764 | — |
反応手順
A mixture of 2-chloro-4-(4-chlorophenyl)-5-[3-(2-methylphenoxy)propyl]oxazole (1.00 g), 2-phenylimidazole (432 mg), potassium carbonate (1.38 g) and N,N-dimethylformamide (10 ml) was stirred at 120-130° C. for 1 hour. The reaction mixture was poured into water (100 ml) and extracted with ethyl acetate (10 ml×2). The organic layer was dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography, and 4-(4-chlorophenyl)-5-[3-(2-methylphenoxy)propyl]-2-(2-phenyl-1-imidazolyl)oxazole was obtained as an oil (512 mg, 39%) from an ethyl acetate-hexane (1:1, v/v)-eluted fraction.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08067453B2 |
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| 出典データセット | uspto-grants-2011_11 |
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| ORD ID | ord-50d7ca600bb34b8f9d8c3af408c69eb7 |
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| 出典メモ | uspto-grants-2011_11 |
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