Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Pentylamine → N-[(2'-nitro-1,1'-biphenyl-4-yl)methyl]-N-pentylamine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Pentylamine | HCID 8060 | — |
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 1,1'-Biphenyl, 4'-(bromomethyl)-2-nitro- | HCID 11779072 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-[(2'-nitro-1,1'-biphenyl-4-yl)methyl]-N-pentylamine | HCID 17860716 | 77% |
반응 단계
n-Amylamine (0.54 g) and potassium carbonate (0.98 g) were suspended in dimethylformamide (3.5 mL), and [[2′-nitro-1,1′-biphenyl-4-yl]methyl] bromide (0.51 g) was added in portions. Four hours later, ethyl acetate (20 mL) was added, and the resulting mixture was washed once with water (40 mL) and twice with brine (90 mL, each). The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was subjected to chromatography on a silica gel column (chloroform/ethyl acetate) to afford N-[(2′-nitro-1,1′-biphenyl-4-yl)methyl]-N-pentylamine as a yellow oil (0.40 g). Yield: 77%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07531576B2 |
| 출처 데이터셋 | uspto-grants-2009_05 |
| ORD ID | ord-2f06d0472f194e309a6ff5cff80b3326 |
| 출처 메모 | uspto-grants-2009_05 |