참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrogen Peroxide | HCID 784 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Methane, dichloromethoxy- | HCID 21004 | — |
| 반응물 | 9-Borabicyclo(3.3.1)nonane | HCID 78966 | — |
| 반응물 | Bicyclo(3.3.1)nonan-9-one | HCID 86638 | — |
| 반응물 | n-Pentylphenyldivinylsilane | HCID 19039141 | — |
| 반응물 | 2-Propanol, 2-methyl-, lithium salt (1:1) | HCID 23664764 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Hexane | HCID 8058 | — |
| 용매 | Tetrahydrofuran hexane | HCID 21883165 | — |
| 생성물 | 4-Pentyl-4-phenyl-4-silacyclohexanone | HCID 11076205 | 91% |
반응 단계
A mixture of 15.9 g of 9-borabicyclo [3.3.1] nonan, 14.8 g of n-pentylphenyldivinylsilane and 150 ml of n-hexane was refluxed for 2 hours and then cooled with ice water. 7.0 ml of borane-dimethylsufide was added to the mixture, which was then heated again and refluxed for 2 hours. After cooling, 16 ml of methanol was added at room temperature and the mixture was stirred for 2 hours at 0° C. 25.0 g of dichloromethylmethyl ether was then dripped into the mixture, followed by also dripping a hexane-tetrahydrofuran (1:1) solution of 1.33M lithium t-butoxide into the mixture. After stirring at room temperature for 2 hours, 80 ml of ethanol, 10 ml of water and 10.0 g of sodium hydroxide were added. Then 80 ml of an aqueous solution of 30% hydrogen peroxide was slowly added. After stirring at room temperature for 2 hours, the organic layer was dried/concentrated to obtain a mixture of the target product and bicyclo [3.3.1] nonan-9-one. They were separated by means of silica-gel chromatography to obtain 15.2 g (yield 91%) of the target product. The target product thus obtained exhibited the same spectra as those of Example 7.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05641431 |
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| 출처 데이터셋 | uspto-grants-1997_06 |
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| ORD ID | ord-f175e89148cd417692d0144a07b154ff |
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| 출처 메모 | uspto-grants-1997_06 |
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