Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Dimethyl Sulfate → 3-(2-Nitro-2-methylpropyl)-7-nitroindole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Dimethyl Sulfate | HCID 6497 | — |
| 반응물 | Indole, 3-((dimethylamino)methyl)-7-nitro- | HCID 15451 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 용매 | 2-Nitropropane | HCID 398 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 3-(2-Nitro-2-methylpropyl)-7-nitroindole | HCID 22014767 | 131% |
반응 단계
The 7-nitrogramine salt (2.0 g, 5.8 mmol) is suspended in a mixture of 2-nitropropane (9.5 mL) and methanol (9.5 mL). Dimethylsulfate (1.09 mL, 11.5 mmol) is added dropwise via syringe, and the resulting yellow solution is stirred at room temperature for 5 minutes. Sodium methoxide (0.62 g, 11.5 mmol) is then added in one portion, and the mixture is stirred overnight at room temperature. The reaction is quenched by addition of saturated NH4Cl solution and ethyl acetate. The aqueous layer is extracted with ethyl acetate, and the combined organic layers are washed with brine, and dried over Na2SO4 to give 1.0 g of 3-(2-nitro-2-methylpropyl)-7-nitroindole (69%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07087635B2 |
| 출처 데이터셋 | uspto-grants-2006_08 |
| ORD ID | ord-8866daba5bfc47cba6e2aaa9a9e6d8c6 |
| 출처 메모 | uspto-grants-2006_08 |