Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Nitropropane → 3-(2-methyl-2-nitropropyl)-1H-indole-4-carboxylic acid methyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Nitropropane | HCID 398 | — |
| 반응물 | Dimethyl Sulfate | HCID 6497 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 반응물 | 3-dimethylaminomethyl-1H-indole-4-carboxylic acid methyl ester hydroiodide | HCID 69518011 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | Ammonium Chloride | HCID 25517 | — |
| 생성물 | 3-(2-methyl-2-nitropropyl)-1H-indole-4-carboxylic acid methyl ester | HCID 69518095 | — |
반응 단계
A 0° C. solution of 3-dimethylaminomethyl-1H-indole-4-carboxylic acid methyl ester hydroiodide (19 g, 52.7 mmol) in 75 ml of methanol and 75 ml of 2-nitropropane is treated with dimethyl sulfate (10 ml, 105.5 mmol) and solid sodium methoxide (6.3 g, 110.6.mmol) sequentially. The resulting mixture is allowed to warm to ambient temperature, and, after stirring overnight, the reaction mixture is diluted with ethyl acetate (300 ml) and saturated aqueous NH4Cl solution (500 ml). The aqueous layer is extracted with ethyl acetate (200 ml), and the combined organic layers are dried over Na2SO4 and concentrated in vacuo to give 3-(2-methyl-2-nitropropyl)-1H-indole-4-carboxylic acid methyl ester in quantitative yield.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07087635B2 |
| 출처 데이터셋 | uspto-grants-2006_08 |
| ORD ID | ord-4866853a2f2646d1ab550d48cec29d92 |
| 출처 메모 | uspto-grants-2006_08 |