참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Chlorotrimethylsilane | HCID 6397 | — |
| 반응물 | Ethyl 3,3-dimethylacrylate | HCID 12516 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | HCID 178478990 | HCID 178478990 | — |
| 촉매 | Cuprous chloride | HCID 62652 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Ethyl 3-cyclohexyl-3-methylbutanoate | HCID 22289815 | — |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06713496B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-34c3090648704563a602edad49707405 |
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| 출처 메모 | uspto-grants-2004_03 |
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