참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | Pentafluorobenzene | HCID 9696 | — |
| 반응물 | HCID 178418306 | HCID 178418306 | — |
| 용매 | Pentane | HCID 8003 | — |
| 생성물 | HCID 178419089 | HCID 178419089 | — |
반응 단계
Inside of a 100 ml volume glass three-neck flask equipped with a 50 ml volume glass dropping funnel, temperature resistor and septum rubber was sufficiently replaced with nitrogen. Into the flask, 5 g (29.8 mmol) of pentafluorobenzene and 30 ml of diethyl ether were charged, of which solution was cooled to -65° C. Thereafter, 12.3 (29.8 mmol) of 16.1 wt. % pentane solution of tert-butyllithium charged into the dropping funnel were added dropwise while making the inner temperature not to exceed -55° C. After the completion of dropwise addition, the reaction mixture was kept at a temperature of -65°~-55° C. with stirring to give pentafluorophenyllithium. To the prepared solution of pentafluorophenyllithium was added 1 mol/L hexane solution (7.45 mL, 7.45 mmol) of boron trihalide at a temperature of -65°~-55° C., kept for 30 minutes at the same temperature with stirring and then the temperature was elevated up to the room temperature to afford a solution of lithium tetrakis(pentafluorophenyl)borate, which was subjected to quantitative determination employing pentafluorotoluene as an inner standard by means of 19FNMR. The yield was 92.3%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05387727 |
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| 출처 데이터셋 | uspto-grants-1995_02 |
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| ORD ID | ord-54ee040f2e78487c891f24c342cb26c6 |
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| 출처 메모 | uspto-grants-1995_02 |
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