참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Bromopentafluorobenzene | HCID 9578 | — |
| 반응물 | Chloropentafluorobenzene | HCID 9579 | — |
| 반응물 | HCID 178418365 | HCID 178418365 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | HCID 178505971 | HCID 178505971 | — |
반응 단계
To a diethyl ether solution of isopropyl magnesium bromide, chloropentafluorobenzene was added at 0 to 40° C. under nitrogen with stirring in a period of thirty minutes, such that the isopropyl magnesium bromide was in 1.03 to 1.05 molar excess of the chloropentafluorobenzene. The mixture was stirred at 47 to 53° C.; after 5 to 10 hours, bromopentafluorobenzene was added to react with the excess isopropyl magnesium bromide, and the mixture was stirred at 25° C. for 1 hour. Any excess bromo-pentafluorobenzene was back-titrated in situ with isopropyl magnesium bromide to form more C6F5MgBr. The yield of C6F5MgBr was 96.1%, and 3.9% C6F5Cl remained, as determined by 19F NMR, using C6H5CF3 as a reference; no trace of iPrMgBr was seen with 1H NMR.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06248265B1 |
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| 출처 데이터셋 | uspto-grants-2001_06 |
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| ORD ID | ord-ad2cee0a57154d0da73629e6118be4f6 |
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| 출처 메모 | uspto-grants-2001_06 |
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