関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Methoxy-3-trimethylsilyloxy-1,3-butadiene | HCID 101051 | — |
| 反応物 | Azetidon | HCID 10935078 | — |
| 触媒 | zinc(II)iodide | HCID 9883512 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | HCID 67627134 | HCID 67627134 | 43% |
反応手順
(3R,4R) 4-acetoxy-3-[(1R)-(1-(tert-butyldimethylsilyloxy)ethyl)]azetidin-2-one (2 g, 56.96 mM) was dissolved in dichloromethane (150 ml) at ambient temperature and 4-methoxy-2-trimethylsilyloxybut-1,3-diene (1.5 ml, 7.65 mM) added followed by zinc iodide (2.2 g, 17 mM). The reaction mixture was shielded from light and stirred for 15 hours. The mixture was then washed with a 5% aqueous solution of sodium bicarbonate (30 ml) and then water (30 ml). The organic phase was dried with magnesium sulphate and the solvent evaporated. The residue was purified by chromatography on silica, eluting with ethyl acetate/dichloromethane (1:1) to give (3S,4R) 3-((1R)-1-(tert-butyldimethylsilyloxy)ethyl)-4-(4-methoxy-2-oxobut-3-en-1-yl)azetidin-2-one (0.96 g, 43%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05719139 |
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| 出典データセット | uspto-grants-1998_02 |
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| ORD ID | ord-6c2c0a33a11a4aa4bc833b045bdf3143 |
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| 出典メモ | uspto-grants-1998_02 |
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