참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethyl Sulfate | HCID 6497 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | methyl 5-tert-butyl-3-nitro-1H-pyrrole-2-carboxylate | HCID 18322358 | — |
| 촉매 | Benzenemethanaminium, N,N,N-tributyl-, bromide | HCID 2724282 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Methyl 5-t-butyl-1-methyl-3-nitropyrrole-2-carboxylate | HCID 18322374 | 57.7% |
반응 단계
Sodium hydroxide (0.21 g, 2.65 mmol, 50% aqueous, 6 equiv) is added to a cold (0-−10° C.) solution of methyl 5-t-butyl-3-nitropyrrole-2-carboxylate (100 mg, 0.44 mmol), benzyltributyl ammonium bromide (158 mg, 0.44 mmol, 1 equiv), and dimethyl sulfate (46 mL, 0.49 mmol, 1.1 equiv) in dichloromethane (1 mL). After 5 min, the cooling bath is removed and the mixture is stirred for 4 h at rt. The reaction mixture is diluted with dichloromethane, washed with water (1×), 10% ammonium acetate (2×), dried (Na2SO4), and concentrated in vacuo to give a bright yellow oil. The residue is purified by flash chromatography (30% hexane in dichloromethane) to give 61 mg of methyl 5-t-butyl-1-methyl-3-nitropyrrole-2-carboxylate as a pale yellow oil which solidifies upon standing (62%). 1H NMR (CDCl3) d 6.47 (s, 1H), 3.92 (s, 3H), 3.80 (s, 3H), 1.38 (s, 9H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06187799B1 |
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| 출처 데이터셋 | uspto-grants-2001_02 |
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| ORD ID | ord-d9ca937f85d649769772bc6c69ef2f13 |
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| 출처 메모 | uspto-grants-2001_02 |
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