関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | {1-[4-(Benzyloxy)phenyl]ethenyl}(tributyl)stannane | HCID 18436367 | — |
| 触媒 | Cuprous chloride | HCID 62652 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 2,3-Di(4-benzyloxy-phenyl)-1,3-butadiene | HCID 18436331 | — |
反応手順
To a cooled solution of tributyl-[1-(4-benzyloxy-phenyl)-vinyl]-stannane (26.2 g, 52.6 mmol) in DMF (180 mL) at 0° C. was added CuCl (8.6 g, 87.7 mmol) and CuCl2 (1.00 g, 8.13 mmol), which was then stirred at 25° C. for 2 h. The reaction mixture was then diluted with ethyl acetate (500 mL) and washed with brine (3×300 mL). The reaction mixture was then dried over MgSO4 and purified by SiO2 (20% ethyl acetate/hexane) to yield 2,3-di(4-benzyloxy-phenyl)-1,3-butadiene.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07183445B2 |
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| 出典データセット | uspto-grants-2007_02 |
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| ORD ID | ord-7d8fd34e7b16494ab4b6b84115eb2720 |
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| 出典メモ | uspto-grants-2007_02 |
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