참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Quintozene | HCID 6720 | — |
| 반응물 | Tetrachlorofluoronitrobenzene | HCID 13099723 | — |
| 반응물 | Dichlorotrifluoronitrobenzene | HCID 22987219 | — |
| 반응물 | Trichloro-difluoronitrobenzene | HCID 22987224 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 1,2-Dichloro-3-fluoro-4-nitrobenzene | HCID 22987215 | 28% |
반응 단계
To a reaction vessel, 0.74 g (2.50 m mol) of pentachloronitrobenzene, 1.77 g (13.00 m mol) of DFI, and 25 ml of acetonitrile were charged and reacted at 84° C. for 2 hours in a nitrogen atmosphere. After finishing the reaction, formation of dichlorotrifluoronitrobenzene (master ion, 245, master ion +2 247, master ion +4 249, base peak 245) was confirmed by GC-MS measurement on the reaction mixture, and the yield was 28.0% by GC analysis. Formation of trichloro-difluoronitrobenzene (master ion 261, master ion +2 263, master ion +4 265, base peak 205) was also confirmed and the yield was 11.3%. Formation of tetrachlorofluoronitrobenzene (master ion 277, master ion +2 279, master ion +4 281, master ion +6 283, base peak 221) was further confirmed and the yield was 9.0%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06458990B1 |
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| 출처 데이터셋 | uspto-grants-2002_10 |
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| ORD ID | ord-0710508926bb49febe6efe6eb59b1241 |
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| 출처 메모 | uspto-grants-2002_10 |
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