참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3,3,3-Trifluoropropyl-trimethoxysilane | HCID 67933 | — |
| 반응물 | Silane hexane | HCID 131717238 | — |
| 반응물 | HCID 178418368 | HCID 178418368 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | 3,3,3-Trifluoropropyl(isobutyl)dimethoxy silane | HCID 19900042 | — |
반응 단계
Under nitrogen, a 500 ml Schlenk flask was cooled to room temperature and charged with 150 ml of diethyl ether and isobutylmagnesium chloride (0.06 mol, 30.24 ml). This was stirred and heated slightly to 30° C. A second Schlenk flask (100 ml) was purged with nitrogen to room temperature and charged with 75 ml hexane and 3,3,3-trifluoropropyltrimethoxy silane (0.0504 mol, 10 ml) and stirred. The silane/hexane solution was added dropwise via cannula to the Grignard/diethyl ether mixture producing a white precipitate midway through the addition. After addition (1.25 hrs.), the reaction mixture was stirred at room temperature for one hour. The flask was fitted with a reflux condenser and the reaction mixture was refluxed for two hours, then allowed to cool to room temperature. The reaction mixture was filtered through a medium porosity frit, using Celite diatomaceous earth and glass wool as a filtering aid. The solids collected weighed 7.55 g (theoretical=4.56 grams of magnesium salts). The slightly cloudy filtrate was kept under nitrogen overnight.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05102842 |
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| 출처 데이터셋 | uspto-grants-1992_04 |
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| ORD ID | ord-25c09710342543ffa93dee71783fd183 |
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| 출처 메모 | uspto-grants-1992_04 |
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