関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetravinylstannane | HCID 66189 | — |
| 反応物 | 2-Chloro-6-(hydroxymethyl)-4-iodo-3-pyridinol | HCID 10684568 | — |
| 触媒 | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 2-Chloro-6-(hydroxymethyl)-4-vinylpyridin-3-ol | HCID 22313278 | 39% |
反応手順
2-Chloro-6-(hydroxymethyl)-4-iodopyridin-3-ol (5.7 g, 20 mmol) is combined with bis (triphenylphosphine) palladium dichloride (1.12 g, 1.6 mmol) in 50 ml DMF under nitrogen. The mixture is treated with tetravinyl tin, is warmed to 60° C. for 6 h followed by 50° C. for 18 h, and at rt for 72 h. The mixture is diluted with 250 ml EtOAc and is extracted with 4×100 ml 2:1:1 water/saturated NaCl/saturated NaHCO3. The organic layer is dried (MgSO4) and is concentrated in vacuo to a yellow oil. The crude material is chromatographed over 200 g SiO2 (230-400 mesh) eluting with 37% EtOAc/hexane. The appropriate fractions are combined and concentrated to afford 1.45 g (39%) of 2-chloro-6-(hydroxymethyl)-4-vinylpyridin-3-ol as a pale yellow solid. MS for C8H8ClNO2 (EI) m/z: 185 (M)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06951868B2 |
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| 出典データセット | uspto-grants-2005_10 |
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| ORD ID | ord-67e925bc1bd74458935cc949ce28af44 |
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| 出典メモ | uspto-grants-2005_10 |
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