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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1176757생성일: 2026년 10월 27일

N-bromobutanimide → Methyl 6-(bromomethyl)pyridine-2-carboxylate

https://huagongshe.com/reaction/1176757

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물Methyl 6-methylpyridine-2-carboxylateHCID 73022—
촉매Benzoyl PeroxideHCID 7187—
용매Carbon TetrachlorideHCID 5943—
생성물Methyl 6-(bromomethyl)pyridine-2-carboxylateHCID 2147171420.2%

반응 단계

6-Bromomethyl-pyridine-2-carboxylic acid methyl ester was prepared according to Wells, G. J. et al. (WO 94/11398): A mixture of 6-methyl-pyridine-2-carboxylic acid methyl ester (6.5 g, 43.0 mmol), benzoyl peroxide (25 mg, 0.1 mmol) and NBS (8.5 g, 47.8 mmol) in carbon tetrachloride (250 mL) was heated at reflux overnight. The reaction mixture was cooled to room temperature, filtered, evaporated, and purified by chromatography on flash silica gel, eluting with 15% ethyl acetate/hexane to give 6-bromomethyl-pyridine-2-carboxylic acid methyl ester (2.0 g, 20%) as a white solid. 1HNMR (CDCl3): δ 8.06 (d, J=8.0 Hz, 1H), 7.87 (dd, J=8.0 Hz, 1H), 7.70 (d, J=8.0 Hz, 1H), 4.65 (s, 2H), 4.02 (s, 3H). MS (APCI+): 231 (45), 235 (42).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07842825B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-d9673c2fb2bc45969f422b986ec8dc57
출처 메모uspto-grants-2010_11