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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1106476생성일: 2026년 10월 24일

5-Bromo-2-methoxypyridine → 5-(3,4-Dimethoxyphenyl)-2-methoxypyridine

https://huagongshe.com/ko/reaction/1106476

반응식

참여 물질

역할이름HCID투입량
반응물5-Bromo-2-methoxypyridineHCID 2734895—
반응물4-TrimethylstannylveratroleHCID 11243535—
촉매HCID 178418397HCID 178418397—
용매DimethylformamideHCID 6228—
생성물5-(3,4-Dimethoxyphenyl)-2-methoxypyridineHCID 18788560—

반응 조건

온도90 °C

반응 단계

A solution of 2.00 g (6.64 mmol) of 4-trimethylstannylveratrole, 2.49 g (13.2 mmol) of 2-methoxy-5-bromopyridine and 370 mg (0.332 mmol) of Pd (PPh3)4 in 30 mL of dry dimethylformamide is flushed thoroughly with nitrogen and heated to 90° C. for 12 hours. The reaction mixture is partitioned between ethyl acetate (150 mL) and water (100 mL). The aqueous layer is back extracted with ethyl acetate (100 mL) and the combined organics are washed with brine (75 mL), dried (MgSO4) and evaporated to give a crude yellow oil. The oil is chromatographed on silica gel (eluting with 95:5 hexane/ethyl acetate and then with 9:1 hexane/ethyl acetate) which gives 5-(3,4-dimethoxy-phenyl)-2-methoxypyridine m.p 83-84° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06057320
출처 데이터셋uspto-grants-2000_05
ORD IDord-ee37cf6de66d45bfac28144ecf2000a9
출처 메모uspto-grants-2000_05