참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 4-Iodobenzonitrile | HCID 76467 | — |
| 반응물 | 2-Octanol, 1,1,1-trifluoro- | HCID 97804 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | p-(1-Trifluoromethyl-heptyloxy)-benzonitrile | HCID 15724839 | — |
반응 단계
Into 100 ml of dry DMF containing 0.86 g of sodium hydride (purity 60%), were added dropwise 3.9 g of R-form oa 1-trifluoromethyl-heptanol, at room temperature with such a speed not causing too rapid generation of hydrogen, to prepare sodium salt (alkoxide) of R-form oa 1-trifluoromethyl-heptanol. After addition was over, stirring was continued further an hour at room temperature, followed by adding thereto 4.80 g of p-iodo-benzonitrile and then refluxing for 2 hours. After cooling, the product was introduced into iced water, and extracted with hexane. The hexane phase was washed subsequently with water, 1N-HCl aqueous solution and then water, followed by purifying with silica gel column to obtain 5.16 g of oily oa p-(1-trifluoromethyl-heptyloxy)- benzonitrile.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05160662 |
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| 출처 데이터셋 | uspto-grants-1992_11 |
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| ORD ID | ord-2b8b5b7465ef4adc9b1eda4352119f95 |
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| 출처 메모 | uspto-grants-1992_11 |
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