참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbon tetrafluoride | HCID 6393 | — |
| 반응물 | 1,1,1,4,5,5,5-Heptafluoro-3-(pentafluoroethyl)-2,4-bis(trifluoromethyl)pent-2-ene | HCID 121670 | — |
| 반응물 | Potassium Fluoride | HCID 522689 | — |
| 반응물 | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| 반응물 | 1,1,1,5,5,5-Hexafluoro-3-[1-(trifluoromethyl)-1,2,2,2-tetrafluoroethyl]-2,4,4-tris(trifluoromethyl)-2-pentene | HCID 22642015 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Perfluoro 4,4-dimethyl-3-isopropyl-2-pentene | HCID 73990785 | — |
반응 단계
1 mmol (450 mg) of perfluoro(3-ethyl-2,4-dimethyl-2-pentene) and 4.0 mmol (568.8 mg) of trifluoromethyltrimethylsilane were weighed into a 10-ml fluororesin-made reaction container, then 1 ml of dimethyl formamide and 0.1 mmol of acidic potassium fluoride (KHF2, 7.8 mg) were added therein. A fluororesin-made magnetic stirrer was placed and the mixture was stirred vigorously for 1 hour at room temperature, and then 1.0 mmol of trifluoromethyltrimethylsilane (142.2 mg) and 0.1 mmol of acidic potassium fluoride (KHF2, 7.8 mg) were added and the mixture was further stirred vigorously for 1 hour at room temperature. After completion of the reaction, the transparent lower perfluorocarbon layer was analyzed by gas chromatography using a capillary column (NB-1, 0.25 μm, 1.5 mm ID×60 m). The yield of the main product perfluoro(2,4,4-trimethyl-3-isopropyl-2-pentene) was 74.5% by weight. As the by-product, perfluoro 4,4-dimethyl-3-isopropyl-2-pentene was obtained at the yield of 25.5% by weight. The starting material perfluoro(3-ethyl-2,4-dimethyl-2-pentene) was consumed completely by the reaction.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06710214B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-13ce255a86bf4c28b9543ff9474bc153 |
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| 출처 메모 | uspto-grants-2004_03 |
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