참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 18-Crown-6 | HCID 28557 | — |
| 반응물 | 6-Chloro-2-fluoro-3-methylphenol | HCID 2773684 | — |
| 반응물 | 4-Bromo-3-fluorobenzonitrile | HCID 15165443 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 4-[(6-Chloro-2-fluoro-3-methylphenyl)oxy]-3-fluorobenzonitrile | HCID 68720989 | 81% |
반응 단계
To a solution of 6-chloro-2-fluoro-3-methylphenol (3.25 g, 20.24 mmol) and 18-crown-6 (0.535 g, 2.024 mmol) in DMSO (40 ml) was added potassium tert-butoxide (20 wt % in THF) (12.49 g, 22.26 mmol) and the reaction mixture was stirred at rt for 30 minutes. Next, 4-bromo-3-fluorobenzonitrile (4.05 g, 20.24 mmol) was added and the reaction mixture stirred at 135° C. for 3 days. The reaction mixture was diluted with EtOAc and washed with water. The solvent was removed and the crude material was purified via silica gel chromatography to give 4-[(6-chloro-2-fluoro-3-methylphenyl)oxy]-3-fluorobenzonitrile (4.56 g, 16.30 mmol, 81% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 8.05 (dd, 1H), 7.59 (d, 1H), 7.35-7.43 (m, 1H), 7.30 (t, 1H), 6.89 (t, 1H), 2.24 (d, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08304419B2 |
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| 출처 데이터셋 | uspto-grants-2012_11 |
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| ORD ID | ord-99238988f1744ea5a6b02c82d1da045c |
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| 출처 메모 | uspto-grants-2012_11 |
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