関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Sodium Tartrate | HCID 9357 | — |
| 反応物 | (2R,3S,4S,5R)-5-(Triethylsilyloxy)-2,3-epoxy-2,4-dimethyl-1-octanol | HCID 57283355 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 反応物 | HCID 178506586 | HCID 178506586 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (2S,3S,4S,5R)-5-(Triethylsilyloxy)-3-hydroxy-2,4-dimethyloctanal | HCID 57313995 | — |
反応手順
(2R,3S,4S,5R)-5-(Triethylsilyloxy)-2,3-epoxy-2,4-dimethyl-1-octanol (21.0 mg, 69.4 μmol) in 300 μl of THF at 0° C. was deprotonated with 1.05 eq of n-butyllithium. After 15 min, 0.1M samarium diiodide (764 μmol, 1.1 eq) was added and the reaction was allowed to warm to 25° C. over night. Then 1 ml of 1/2 saturated Rochelle's salt was added, stirred an additional 1 h, and poured onto 5 ml of Et2O and 1 ml of H2O. The layers were separated, extracted with ether (3×5 ml), washed with 5% NaHCO3 (2×1 ml), brine (1×1 ml), dried over MgSO4 and concentrated to give 31 crude.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05426206 |
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| 出典データセット | uspto-grants-1995_06 |
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| ORD ID | ord-886f87c09f3e4a15999176d8eab283ce |
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| 出典メモ | uspto-grants-1995_06 |
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