참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Triisopropylsilyl trifluoromethanesulfonate | HCID 2724529 | — |
| 반응물 | 4-(2,4,5-Trifluorophenyl)cyclohexanone | HCID 57424362 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Triisopropyl{[4-(2,4,5-trifluorophenyl)cyclohex-1-en-1-yl]oxy}silane | HCID 67065786 | — |
반응 단계
A three-neck flask (1 L) containing a stirred solution of 4-(2,4,5-trifluorophenyl)cyclohexanone (15.8 g) in dichloromethane (160 mL) under a nitrogen atmosphere was cooled to 0° C. and then treated with triethylamine (22 mL) followed by triisopropylsilyl trifluoromethanesulfonate (25.4 g) while maintaining the temperature below 5° C. The solution was stirred at 0° for 30 min and then allowed to rise to ambient temperature over a period of 0.5 h. It was then treated with saturated aqueous ammonium chloride solution. The organic layer was separated, dried over anhydrous magnesium sulfate and evaporated. The crude product was chromatographed (silica gel, 3% ether in hexane) to yield the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07906649B2 |
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| 출처 데이터셋 | uspto-grants-2011_03 |
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| ORD ID | ord-d4f395ba346b46dc933b09a0407c3940 |
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| 출처 메모 | uspto-grants-2011_03 |
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