참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylamine | HCID 7912 | — |
| 반응물 | Hexachloroacetone | HCID 8303 | — |
| 반응물 | 1-Bromo-2,4-difluorobenzene | HCID 67674 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-Bromo-3-chloro-2,4-difluorobenzene | HCID 2773256 | — |
반응 단계
To a solution of 19 ml (0.135 mole) of diisopropylamine in 125 ml of tetrahydrofuran (THF) cooled at −20° C. is added 80 ml of n-butyllithium (1.6 M in hexane). The temperature is raised to 0° C. for 5 minutes and lowered to −78° C. Then 25 g (0.129 mole) of 2,4-difluoro-bromobenzene is then added and the reaction is stirred at −65° C. for 2 hours. Then, 25 ml (0.164 mole) of hexachloroacetone is added and the solution is warmed at room temperature. After evaporation of the solvent, the residue is distilled under vacuum to give the desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06387928B1 |
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| 출처 데이터셋 | uspto-grants-2002_05 |
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| ORD ID | ord-e8276d98556848c5bbe4110e2f9a6dd7 |
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| 출처 메모 | uspto-grants-2002_05 |
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