참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyrazole | HCID 1048 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 4-Nitrophenethyl bromide | HCID 79266 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 1-[2-(4-nitrophenyl)ethyl]-1H-pyrazole | HCID 63810942 | 8% |
반응 단계
A mixture of 1-(2-bromoethyl)-4-nitrobenzene (18.7 g), pyrazole (5.53 g) and potassium hydroxide (4.56 g) was stirred at 140° C. for 8 min. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography to give 1-[2-(4-nitrophenyl)ethyl]-1H-pyrazole (1.37 g, 8%) as crystals from a fraction eluted with hexane-ethyl acetate (1:2, v/v). Recrystallization thereof from ethyl acetate-hexane gave yellow prism crystals. melting point: 92-93° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07423159B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-63a98340bebf4655b901d80ba0441790 |
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| 출처 메모 | uspto-grants-2008_09 |
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