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HRID 395624作成日:2026年10月26日
Dimethylformamide → 4-(4-Chlorophenyl)-2-(2-isopropyl-1-imidazolyl)-5-[3-(2-methylphenoxy)propyl]oxazole
https://huagongshe.com/reaction/395624
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 1H-Imidazole, 2-(1-methylethyl)- | HCID 123457 | — |
| 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)-2-(2-isopropyl-1-imidazolyl)-5-[3-(2-methylphenoxy)propyl]oxazole | HCID 18174757 | — |
反応手順
A mixture of 2-chloro-4-(4-chlorophenyl)-5-[3-(2-methylphenoxy)propyl]oxazole (1.00 g), 2-isopropylimidazole (661 mg), potassium carbonate (830 mg) 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 then concentrated. The residue was subjected to silica gel column chromatography, and 4-(4-chlorophenyl)-2-(2-isopropyl-1-imidazolyl)-5-[3-(2-methylphenoxy)propyl]oxazole was obtained as an oil (333 mg, 28%) 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 | US06605629B1 |
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| 出典データセット | uspto-grants-2003_08 |
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| ORD ID | ord-272344a9f1f0468898b6c4935bfa6305 |
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| 出典メモ | uspto-grants-2003_08 |
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