참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Acetic acid, chloro-, pentyl ester | HCID 138488 | — |
| 반응물 | Phenol, 2-chloro-4-fluoro-5-nitro- | HCID 158655 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4-Chloro-2-fluoro-5-(pentyloxycarbonylmethyloxy)nitrobenzene | HCID 14617849 | 77.3% |
반응 단계
A mixture of 2-chloro-4-fluoro-5-nitrophenol (100 g), anhydrous potassium carbonate (86.6 g) and dimethylformamide (500 g) was heated at 50° C., and amyl 2-chloroacetate (90.2 g) was dropwise added thereto in 30 minutes, followed by allowing to stand at 60° C. for 4 hours. The reaction mixture was cooled to room temperature, and water (1500 g) was added thereto, followed by extraction with ethyl acetate (1500 g). The organic layer was separated, washed with water and concentrated under reduced pressure. The residue was distilled under reduced pressure to give 4-chloro-2-fluoro-5-(pentyloxycarbonylmethyloxy)nitrobenzene (Compound (III)) (129 g) as a pale yellow oil. Yield, 77%. b.p., 160°-165° C./0.7 mmHg.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04985570 |
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| 출처 데이터셋 | uspto-grants-1991_01 |
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| ORD ID | ord-4e61f74ca11c4edcacad9de6e4ffc51c |
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| 출처 메모 | uspto-grants-1991_01 |
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