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HRID 1518962생성일: 2026년 10월 27일

3-Bromo-2-chloro-6-methylpyridine → 3-Bromo-2-methoxy-6-methylpyridine

https://huagongshe.com/reaction/1518962

반응식

참여 물질

역할이름HCID투입량
반응물3-Bromo-2-chloro-6-methylpyridineHCID 2734418—
반응물Sodium MethoxideHCID 10942334—
용매TetrahydrofuranHCID 8028—
생성물3-Bromo-2-methoxy-6-methylpyridineHCID 2195258746.1%

반응 단계

To a cooled (0° C.) solution of 3-bromo-2-chloro-6-methylpyridine (300 mg, 1.45 mmol) in tetrahydrofuran (20 mL), add sodium methoxide (1.57 g, 29 mmol), slowly with stirring. Allow the mixture to warm to ambient temperature and stir overnight. Add additional sodium methoxide (500 mg) and stir at 100° C. overnight. Quench with water (20 mL), extract three times with ethyl acetate (30 mL). Combine the organics and wash with water then brine, and dry over sodium sulphate. Filter and concentrate to give the title product as a yellow solid (135 mg, 46%). 1HNMR (MeOH-d4): δ 7.72 (d, 1H), 6.70 (d, 1H), 3.93 (s, 3H), 2.38 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09073856B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-8d366de7535d4acfbe9c4cc74166b2f9
출처 메모uspto-grants-2015_07