関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Crotyl chloride | HCID 11589 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Lithium iodide | HCID 66321 | — |
| 反応物 | 2-Chloro-3-hydroxy-4-iodo-6-(1-hydroxyethyl)-pyridine | HCID 10709299 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | HCID 54217396 | HCID 54217396 | 89% |
反応手順
2-Chloro-3-hydroxy-6-(1-hydroxyethyl)-4-iodo-pyridine (4.49 g, 15 mmole) was dissolved in 25 ml dry dimethylformamide in an oven dried 50 ml two neck round bottom flask under nitrogen. The solution was cooled to 0° C., was treated with sodium hydride (600 mg, 15 mmole), and the mixture was stirred 1 h at room temperature. The mixture was treated with crotyl chloride (1.6 ml, 16.5 mmole) and one crystal of lithium iodide and the reaction mixture was stirred 20 h at room temperature. The reaction mixture was diluted with 100 ml ethyl acetate, was washed with 4×50 ml 50% saturated 1:1 sodium chloride/sodium bicarbonate, and was dried over anhydrous magnesium sulfate/potassium carbonate. The dried organics were concentrated in vacuo to a yellow oil which was crystallized from hexane to give 4.72 g (89%) of 3-(2-butenyloxy)-2-chloro-6-(1-hydroxyethyl)-4-iodo-pyridine as a white solid (Melting Point: 61-62.50° C.).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06043248 |
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| 出典データセット | uspto-grants-2000_03 |
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| ORD ID | ord-ffa29632cbe04195bf36b7f43db2f177 |
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| 出典メモ | uspto-grants-2000_03 |
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