참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | p-Xylyl bromide | HCID 7721 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | HCID 178526745 | HCID 178526745 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-(4-methylbenzyl)-3-nitro-1H-pyrazole | HCID 7010174 | 82.2% |
반응 단계
To a solution of 3-nitro-1H-pyrazole (prepared in example 3, 200 mg, 1.77 mmol) in anhydrous N,N-dimethylformamide (2 mL), a 60% dispersion of sodium hydride in mineral oil 92 mg, 2.30 mmol) was added while stirring under nitrogen. After the effervescence ceased and the mixture was stirred for additional 20 min, 4-methylbenzylbromide (426 mg, 2.30 mmol) was added. The mixture was continued to stir under nitrogen for an additional 2 h. The solvent was removed in vacuo and purification by ISCO flash column chromatography (Teledyne Isco RediSep Flash Column 40 g; 2% methanol/methylene chloride to 5% methanol/methylene chloride) afforded 1-(4-methyl-benzyl)-3-nitro-1H-pyrazole (316 mg, 82%) as a white solid: H1-NMR (400 MHz, CDCl3) δ: 2.36 (3H, s), 5.32 (2H, s), 6.87 (1H, d, J=2.3 Hz), 7.19 (4H, s), 7.34 (1H, d, J=2.3 Hz).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07935699B2 |
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| 출처 데이터셋 | uspto-grants-2011_05 |
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| ORD ID | ord-0a74d6e706e94597b81e0c482d3ffd78 |
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| 출처 메모 | uspto-grants-2011_05 |
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