関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Imidazole | HCID 795 | — |
| 反応物 | rel-(1R,2S)-2-Phenylcyclohexanol | HCID 102793 | — |
| 反応物 | Triisopropylsilyl chloride | HCID 139400 | — |
| 反応物 | Benzyloxyacetyl chloride | HCID 177085 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Pentane | HCID 8003 | — |
| 生成物 | (-)-(1R,2S)-2-phenyl-1-cyclohexyl hydroxyacetate | HCID 10059921 | 95% |
反応手順
To obtain 1c(-), a solution of (-)-(1R,2S)-2-phenyl-1-cyclohexyl hydroxyacetate (851 mg, 3.63 mmol) was prepared through esterification of benzyloxyacetyl chloride with (-)-(1R,2S)-2-phenyl-1-cyclohexanol followed by hydrogenolysis. Then, triisopropylsilyl chloride (840 mg, 4.36 mmol) and imidazole (618 mg, 9.08 mmol) in dimethylformamide (DMF) (1.7 mL) was stirred at room temperature for 12-20 hours. The mixture was poured into pentane (25 mL), and washed with water and brine. The combined organic layers were dried over anhydrous MgSO4 and concentrated in vacuo. The crude product was subjected to a purification on a short silica gel column using hexane/chloroform (3/1) as the eluant to give pure 1c(-) (1.35 g, 95% yield) as a colorless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05294737 |
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| 出典データセット | uspto-grants-1994_03 |
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| ORD ID | ord-8c8b239c359f4197a5536012d4027c08 |
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| 出典メモ | uspto-grants-1994_03 |
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