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HRID 230847作成日:2026年10月27日
Methyltriphenylphosphonium iodide → N-(5-Chloro-3-methylidene-2,3-dihydro-1-benzofuran-4-yl)-2,2,2-trifluoroacetamide
https://huagongshe.com/reaction/230847
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Methyltriphenylphosphonium iodide | HCID 638159 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 反応物 | N-(5-Chloro-3-oxo-2,3-dihydro-1-benzofuran-4-yl)-2,2,2-trifluoroacetamide | HCID 57763220 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | N-(5-Chloro-3-methylidene-2,3-dihydro-1-benzofuran-4-yl)-2,2,2-trifluoroacetamide | HCID 57763270 | — |
反応手順
To a mixture of potassium tert-butoxide (2.0) and methyltriphenylphosphonium iodide (7.1 g) was added dry toluene (70 ml) and the mixture stirred at room temperature for 30 min, then heated under reflux for 30 min. The mixture was cooled to room temperature, a solution of Intermediate 22 (1.0 g) in toluene (30 ml) added dropwise and the mixture heated under reflux for 30 min. The mixture was cooled and quenched by the dropwise addition of saturated ammonium chloride solution. The mixture was partitioned between ethyl acetate and water and the organic phase washed with water. The combined aqueous layers were re-extracted with ethyl acetate and the combined organic layers dried over sodium sulphate and concentrated in vacuo to give a dark brown oil. Purification by column chromatography on silica gel, eluting with 10% ethyl acetate in cyclohexane, gave the title compound as a rose coloured solid (0.5 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07566786B2 |
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| 出典データセット | uspto-grants-2009_07 |
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| ORD ID | ord-1368f349ddde440a9dc52c3212aec625 |
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| 出典メモ | uspto-grants-2009_07 |
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