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HRID 1018374作成日:2026年10月26日
Water → 3-{2-[5-(2-Adamantan-1-yl-ethyl)-1-methyl-2-o-tolyl-1H-imidazol-4-yl]-vinyl}-benzoic acid methyl Ester
https://huagongshe.com/reaction/1018374
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Phosphonium, [[3-(methoxycarbonyl)phenyl]methyl]triphenyl-, bromide | HCID 10051285 | — |
| 反応物 | 5-(2-Adamantan-1-yl-ethyl)-1-methyl-2-o-tolyl-1H-imidazole-4-carbaldehyde | HCID 18405418 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 3-{2-[5-(2-Adamantan-1-yl-ethyl)-1-methyl-2-o-tolyl-1H-imidazol-4-yl]-vinyl}-benzoic acid methyl Ester | HCID 70160899 | — |
反応手順
Sodium hydride (60% dispersion in oil) (122 mg, 3.05 mmol) was added to an ice cooled suspension of 3-methoxycarbonyl-benzyl-triphenylphosphonium bromide (1.25 g, 2.54 mmol) in THF (5 ml). The yellow suspension was stirred at room temperature for 10 min, cooled to 0° C. and the solution of the product of step b (7686 mg, 2.12 mmol) in THF (5 ml) was added. The suspension was allowed to warm to room temperature and stirred for 72 h. Water (2 ml), then ethyl acetate (40 ml) were added. The organic phase was washed with water (30 ml), brine (30 ml), dried (MgSO4) and the solvent was evaporated. The crude product was purified by flash column chromatography (silica, hexane/ethyl acetate 5:2) to afford the product as 2:1 mixture of trans/cis isomers (778 mg, 74%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06479531B1 |
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| 出典データセット | uspto-grants-2002_11 |
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| ORD ID | ord-67e3a5df10fa4d52a1bf856fb10494f4 |
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| 出典メモ | uspto-grants-2002_11 |
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