関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Chlorotrimethylsilane | HCID 6397 | — |
| 反応物 | Ethyl 3,3-dimethylacrylate | HCID 12516 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | HCID 178478990 | HCID 178478990 | — |
| 触媒 | Cuprous chloride | HCID 62652 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Ethyl 3-cyclohexyl-3-methylbutanoate | HCID 22289815 | — |
反応手順
Trimethylsilyl chloride (1.3 ml, 10.2 mmol), copper (i) chloride (30 mg, 0.3 mmol) and cyclohexylmagnesium chloride (4.6 ml, 2N in diethyl ether, 9.2 mmol) were added slowly to an ice-cooled solution of ethyl 3,3-dimethylacrylate (1 g, 8.5 mmol) in tetrahydrofuran (10 ml). The solution was stirred for 10 minutes, then allowed to warm to room temperature and stirred for an hour. Saturated aqueous ammonium chloride solution (10 ml) was added and the mixture was partitioned between water (10 ml) and diethyl ether (20 ml). The layers were separated and the aqueous phase was extracted with diethyl ether (2×10 ml). The combined organic extracts were dried (MgSO4) and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel using ethyl acetate:pentane(5:95) as eluant to afford the title compound, 1.2 g. 1H-NMR (CDCl3, 400 MHz) δ: 0.75 (m, 8H), 1.05-1.28 (m, 7H), 1.62 (m, 1H), 1.78 (m, 4H), 2.20 (s, 2H), 4.10 (q, 2H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06958402B2 |
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| 出典データセット | uspto-grants-2005_10 |
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| ORD ID | ord-721a5005b1764fcd8c2587feb0b851f1 |
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| 出典メモ | uspto-grants-2005_10 |
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