関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrogen Peroxide | HCID 784 | — |
| 反応物 | Borane | HCID 6331 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | ethyl {3-[(2E)-but-2-en-1-yl]-2-oxocyclohexyl}acetate | HCID 58986251 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Sodium chloride; water | HCID 57417360 | — |
| 生成物 | 2-Ethyl (2-ethyl-7a-hydroxyoctahydro-1-benzofuran-7-yl)acetate | HCID 58986239 | — |
反応手順
To a stirred solution of ethyl {3-[(2E)-but-2-en-1-yl]-2-oxocyclohexyl}acetate (565 mg, 2.37 mmol) in tetrahydrofuran (20 ml) at 0° C. was added borane.tetrahydrofuran complex (1 M in tetrahydrofuran, 3.56 ml, 3.56 mmol) and the reaction allowed to stir at 0° C. for 35 min. Sodium hydroxide (4N, 5.6 ml) and hydrogen peroxide (5.6 ml) were added and the reaction allowed to stir at room temperature for 1 h. Diluted with brine, then extracted three times with dichloromethane. The combined organics were washed twice with brine, dried over sodium sulfate, concentrated in vacuo and purified by column chromatography (50% EtOAc/hexanes). The desired title compound (345 mg) was obtained as a colourless oil as a complex mixture of diastereomers.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07728022B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-edb649375269480abe9d8dfb97e80e8b |
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| 出典メモ | uspto-grants-2010_06 |
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