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 | — |
반응 단계
To a cold (0-10° C.) solution of methyl 5-tert-butyl-3-nitropyrrole-2-carboxylate (0.100 g, 0.44 mmol), benzyltributylammonium bromide (0.16 mg, 0.44 mmol, 1 equiv), and dimethyl sulfate (46 μL, 0.49 mmol, 1.1 equiv) in CH2Cl2 (1 mL) was added a 50% NaOH solution (0.21 g, 2.65 mmol, 6 equiv). After 5 min, the cooling bath was removed and the mixture was stirred at room temp. for 4 h. The reaction mixture was diluted with CH2Cl2, washed with water and a 10% NH4OAc solution (2x), dried (Na2SO4), and concentrated under reduced pressure to give a bright yellow oil. The oil was purified by flash chromatography (70% CH2Cl2/hexane) to give methyl 5-tert-butyl-1-methyl-3-nitropyrrole-2-carboxylate as a pale yellow oil which solidifies upon standing (0.061 g, 62%): 1H NMR (CDCl3) δ1.38 (s, 9H)., 3.80 (s, 3H), 3.92 (s, 3H), 6.47 (s, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06344476B1 |
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| 출처 데이터셋 | uspto-grants-2002_02 |
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| ORD ID | ord-b2d3ecb9c20f410bad57fd90f4b50329 |
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| 출처 메모 | uspto-grants-2002_02 |
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