참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Phosphine, triphenyl-, hydrobromide | HCID 517696 | — |
| 반응물 | [1,1'-Bicyclohexyl]-4-one,4'-propyl-, | HCID 4354185 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 4-(4-Propylcyclohexyl)cyclohexane | HCID 17884097 | 56% |
반응 단계
Into a three-necked flask equipped with a dropping funnel, a three-way cock and a thermometer was placed (2-(1,3-dioxan)-2-yl)ethyl)triphenylphosphonium bromide (12.3 g, 27 mmols), followed by adding tetrahydrofuran (50 ml), suspending, stirring under ice cooling till the liquid temperature reached 10° C. The reaction mixture is added potassium t-butoxide (3.0 g, 27 mmols), followed by elevating the temperature up to room temperature under ice cooling for one hour, stirring for one hour, dropwise adding a tetrahydrofuran (10 ml) solution of 4-(4-propylcyclohexyl)cyclohexanone (15.6 g, 25 mmols) over 30 minutes from the dropping funnel, further stirring the reaction mixture for 5 hours after completion of the dropwise addition, adding ether (50 ml), allowing to stand for one hour, filtering off deposited insoluble substance, concentrating the filtrate under reduced pressure, isolating and purifying the resulting pale brown oily substance by means of silica gel column chromatography and recrystallizing from ethanol, to obtain 1-(2-(1,3-dioxan)-2-yl)ethylidene)-4-(4-propylcyclohexyl)cyclohexane (4.5 g, 14 mmols).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05609791 |
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| 출처 데이터셋 | uspto-grants-1997_03 |
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| ORD ID | ord-b6001f375b1c4dde9bc2c80ccc1b1963 |
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| 출처 메모 | uspto-grants-1997_03 |
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