참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | 2-Bromoethanol | HCID 10898 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 3,5-Dibromo-4-nitro-1H-pyrazole | HCID 13707994 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3,5-Dibromo-1-(2'-hydroxyethyl)-4-nitropyrazole | HCID 13007236 | — |
반응 단계
A solution of 3,5-dibromo-4-nitropyrazole (2) (11.0 g, 41 mmol) in DMF (52 ml) was added dropwise over 20 min to a stirred solution of NaH (1.76 g, 46 mmol; 60% dispersion in oil, prewashed with hexane under an inert atmosphere) in DMF (88 ml). After stirring for 10 minutes, a solution of 2-bromoethanol (6.4 g, 49 mmol) in DMF (14 ml) was added dropwise over 10 minutes. The reaction mixture was heated to 80° C. for 2 hours and then the DMF was evaporated off under reduced pressure. A mixture of DCM/water (100 ml, 1/1) is added to the residue and the organic phase is washed with water (50 ml). The organic phase was dried over Na2SO4 and the solvent was evaporated off under reduced pressure. The crude brown solid obtained was subsequently purified by column chromatography (5%/95% EtOAc/hexane). The yellow solid product (3.4 g) was recrystallized from a mixture of toluene/hexane (20 ml, 55%/45%) to give the 2-(3,5-dibromo-4-nitropyrazol-1-yl)ethanol (3) in the form of a white solid (2.8 g, 22%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07091350B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-2a84430a84bb465c92f452a6b69a439a |
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| 출처 메모 | uspto-grants-2006_08 |
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