Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Azobisisobutyronitrile → 3-Methoxy-2-nitro-6-pyridylmethyl bromide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Azobisisobutyronitrile | HCID 6547 | — |
| 반응물 | N-bromobutanimide | HCID 67184 | — |
| 반응물 | 3-Methoxy-6-methyl-2-nitropyridine | HCID 2727965 | — |
| 용매 | Carbon Tetrachloride | HCID 5943 | — |
| 생성물 | 3-Methoxy-2-nitro-6-pyridylmethyl bromide | HCID 14405124 | 21.3% |
반응 단계
A catalytic amount of α,α'-azobis(isobutyronitrile) was added to 3-methoxy-6-methyl-2-nitropyridine (described in Acta Chem. Scand., vol. 23, pages 1791-1796) (7.1 g), N-bromosuccinimide (7.1 g) and carbon tetrachloride (80 ml), and the mixture was refluxed for 16 hours. After the reaction, while the reaction mixture was still hot, it was suction-filtered to separate the insoluble succinimide. The filtrate was cooled to room temperature whereupon the unreacted 3-methoxy-6-methyl-2-nitropyridine precipitated as crystals. The crystals were separated by filtration. The residue was concentrated and then vacuum distilled to give 3-methoxy-2-nitro-6-pyridylmethyl bromide (2.1 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04772620 |
| 출처 데이터셋 | uspto-grants-1988_09 |
| ORD ID | ord-f9c7e3be90e044b4ae9244e313e2dd74 |
| 출처 메모 | uspto-grants-1988_09 |