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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 450179생성일: 2026년 10월 24일

2-Chloro-5-nitropyrimidine → 2-Methoxy-5-nitropyrimidine

https://huagongshe.com/ko/reaction/450179

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloro-5-nitropyrimidineHCID 82544—
반응물Sodium MethoxideHCID 10942334—
용매MethanolHCID 887—
생성물2-Methoxy-5-nitropyrimidineHCID 352900134.3%

반응 단계

To a solution of sodium methoxide (0.090 g of sodium) in MeOH (12 mL) was added 0.486 g (3.03 mmol) of 2-chloro-5-nitropyrimidine, and the mixture was heated under reflux for 1 hr. After cooling, the mixture was concentrated in vacuo, extracted with EtOAc, and washed with water. The aqueous layer was extracted with CHCl3 and the combined organic layers were dried (Na2SO4), and concentrated, to give 0.347 g (75% yield) of 2-methoxy-5-nitropyrimidine as a yellow powder: 1H NMR (CDCl3) δ9.31 (s, 2H), 4.17 (s, 3H); LCMS (APCI+) m/z: 156 (MH+, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08486939B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-160f4f9dca0f416a938b965dced57a0a
출처 메모uspto-grants-2013_07