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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1037305생성일: 2026년 10월 26일

Methyl iodide → 2-Chloro-3-methoxypyridine

https://huagongshe.com/reaction/1037305

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물2-Chloro-3-pyridinolHCID 81136—
반응물Sodium MethoxideHCID 10942334—
용매DimethylformamideHCID 6228—
생성물2-Chloro-3-methoxypyridineHCID 10425279%

반응 단계

To a stirred solution of 2-chloro-3-hydroxypyridine (25.4 g, 196 mmol) in dry DMF (250 mL), at 0° C., was added sodium methoxide (11.5 g, 213 mmol). After 5 min, the reaction mixture was allowed to warm to RT. After 1 hour, the mixture was cooled to 0° C. and iodomethane (24 mL, 386 mmol) was added. The reaction mixture was stirred at 0° C. for 5 minutes, before allowing to warm to RT. After 2 hours, the reaction mixture was concentrated under reduced pressure. The resultant residue was partitioned between diethyl ether and water. The aqueous phase was isolated and extracted twice with diethyl ether. The combined organic extracts were washed with water, brine, dried (Na2SO4), filtered and concentrated in vacuo to give the title compound (22.2 g, 79%) as an orange solid. LCMS (Method A): RT=2.76 min, [M+H]+=144/146.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08546376B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-c08ab2ebc3404938a14ddafb0f6dc8c4
출처 메모uspto-grants-2013_10