참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Phenol, 2-chloro-4-fluoro-5-nitro- | HCID 158655 | — |
| 반응물 | Cyclopentyl 4-methylbenzene-1-sulfonate | HCID 317685 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 2-Fluoro-4-chloro-5-cyclopentyloxynitrobenzene | HCID 19374470 | 92.6% |
반응 단계
A solution of 2-fluoro-4-chloro-5-hydroxynitrobenzene (7.1 g, 37.1 mmol) and potassium carbonate (5.1 g, 37.1 mmol) in acetonitrile (300 ml) was stirred for 2 hours at a refluxing temperature. Cyclopentyl p-toluenesulfonate (10.3 g, 40.8 mmol) was added thereto, followed by stirring further for 2 hours under refluxing. After completion of the reaction, the solvent was distilled off under reduced pressure from the reaction mixture, in hydrochloric acid (300 ml) was added thereto, and the mixture was extracted with ethyl acetate (100 ml×3 times). The organic layer was washed with an aqueous solution of sodium bicarbonate and water, dried, and the solvent was distilled off under reduced pressure to obtain 2-fluoro-4-chloro-5-cyclopentyloxynitrobenzene as a yellow solid (8.93 g, 34.3 mmol, 92.6% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05424277 |
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| 출처 데이터셋 | uspto-grants-1995_06 |
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| ORD ID | ord-0b1ea39f652a4ec0b1ad722b5587f73d |
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| 출처 메모 | uspto-grants-1995_06 |
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