関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 反応物 | Cinnamic Acid | HCID 444539 | — |
| 反応物 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Ethyl-3-oxo-5-phenylpent-4-enoate | HCID 11053129 | 57% |
反応手順
Trans-cinnamic acid (5 mmol, manufactured by Fluka), 1,1′-carbonyl diimidazole (892 mg, 5.5 mmol, manufactured by Aldrich) and tetrahydrofuran (10 mL) were charged in a 25 mL round-bottom flask, followed by stirring at room temperature for 1 hour. 1M lithium bis(trimethylsilyl)amide (10 mL, 10 mmol, manufactured by Aldrich), ethyl acetate (977 μL, 10 mmol), and tetrahydrofuran (10 mL) were added to thereto, followed by stirring at −78° C. for 1 hour. Two solutions were mixed, gradually warmed and stirred at room temperature for 1 hour. A saturated ammonium chloride aqueous solution (50 mL) and ethyl acetate (50 mL) were added thereto, followed by separation of layers into two layers and washing with distilled water and saline. The organic layer was dried over anhydrous sodium sulfate and separated by column chromatography (n-Hex/EtOAc=15/1 (v/v)) to afford Compound 8a.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08637674B2 |
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| 出典データセット | uspto-grants-2014_01 |
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| ORD ID | ord-63a8dc5c60cf45ba8f8ce65ff454c2f0 |
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| 出典メモ | uspto-grants-2014_01 |
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