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HRID 23318作成日:2026年10月24日
(E)-1,3-Dichloropropene → (E)-2-(1-Methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methyl-6-(3-chloroprop-2-enyloxy)pyridine
https://huagongshe.com/ja/reaction/23318
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | (E)-1,3-Dichloropropene | HCID 24726 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | HCID 178429419 | HCID 178429419 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 溶媒 | Ethyl acetate pentane | HCID 22335286 | — |
| 生成物 | (E)-2-(1-Methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methyl-6-(3-chloroprop-2-enyloxy)pyridine | HCID 15477174 | 52.3% |
反応手順
A mixture of 6-hydroxy-2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methylpyridine (0.9 g, 3.3 mmol) and NaH (60% in oil, 0.16 g, 4 mmol) in acetonitrile (20 ml) and DMF (1 ml) is stirred for 10 min at ambient temperature and (E)-1,3-dichloropropene (0.4 g, 3.6 mmol) is added. After stirring for 60 h at ambient temperature, the remaining NaH is deactivated and the resulting mixture is diluted with pentane/ethyl acetate (by volume ration 1/1) and filtered through a bed of silica gel. The filtrate is washed with water. The organic layer is dried with anhydrous magnesium sulfate, filtered and evaporated in vacuo. Purification by flash chromatography (silica gel: pentane/ethyl acetate 9/1 v/v) yields the title compound (0.6 g, 52% yield) as an colorless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06852673B2 |
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| 出典データセット | uspto-grants-2005_02 |
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| ORD ID | ord-1a51b45be5a940eea36ea661e6865feb |
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| 出典メモ | uspto-grants-2005_02 |
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