돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 622708생성일: 2026년 10월 25일

Azobisisobutyronitrile → 3-Methoxy-2-nitro-6-pyridylmethyl bromide

https://huagongshe.com/reaction/622708

반응식

참여 물질

역할이름HCID투입량
반응물AzobisisobutyronitrileHCID 6547—
반응물N-bromobutanimideHCID 67184—
반응물3-Methoxy-6-methyl-2-nitropyridineHCID 2727965—
용매Carbon TetrachlorideHCID 5943—
생성물3-Methoxy-2-nitro-6-pyridylmethyl bromideHCID 1440512421.3%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04772620
출처 데이터셋uspto-grants-1988_09
ORD IDord-f9c7e3be90e044b4ae9244e313e2dd74
출처 메모uspto-grants-1988_09