참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | p-Fluoronitrobenzene | HCID 9590 | — |
| 반응물 | Bromine | HCID 24408 | — |
| 반응물 | Benzene, [1-[(trimethylsilyl)oxy]ethenyl]- | HCID 117406 | — |
| 반응물 | Tris(dimethylamino)sulfonium difluorotrimethylsilicate | HCID 9795567 | — |
| 반응물 | Sodium Bisulfite | HCID 23665763 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Cyclohexane | HCID 8078 | — |
| 생성물 | 2-(2-Nitro-5-fluorophenyl)-1-phenylethanone | HCID 13507910 | — |
반응 단계
To a solution of 2.12 mL (20 mmol) of 4-fluoronitrobenzene and 4.12 mL (21 mmol) of [(1-phenyl-1-ethenyl)oxy]trimethylsilane in 30 mL of THF at -78° C. was added 5.502 g (20 mmol) of TASF dissolved in 6 mL of acetonitrile and 5 mL of THF. After stirring for 3 hrs at -78° C., 1.00 mL (19.50 mmol) of bromine in 5 mL of cyclohexane was added dropwise. After being stirred for 15 min at -78° C., the mixture was warmed to room temperature and stirred further for 30 min. Thirty mL of saturated sodium bisulfite was added, and the product was extracted into four 60 mL portions of ether. The organic phase was washed with saturated sodium chloride, dried, and concentrated. Chromatography on silica using 30% ether/hexanes yielded the expected product. The yield was 1.660 g (38%) of product, which was an oil. The product material was analyzed by infrared spectroscopy, nuclear magnetic resonance spectroscopy, and mass spectrometry.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05164499 |
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| 출처 데이터셋 | uspto-grants-1992_11 |
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| ORD ID | ord-094239ba94bc4dcca939ac2ca53597b2 |
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| 출처 메모 | uspto-grants-1992_11 |
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