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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77804생성일: 2026년 10월 23일

Sodium hydride → 2-(4-Bromo-benzyloxy)-6-methyl-pyridine

https://huagongshe.com/ko/reaction/77804

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물4-Bromobenzyl alcoholHCID 70119—
반응물2-Fluoro-6-methylpyridineHCID 96090—
용매DimethylformamideHCID 6228—
생성물2-(4-Bromo-benzyloxy)-6-methyl-pyridineHCID 5925547881%

반응 단계

To a solution of (4-bromo-phenyl)-methanol (4.54 g, 24.3 mmol) in N,N-dimethylformamide (50 mL) was added sodium hydride (999 mg, 25 mmol, 60% in oil) under nitrogen atmosphere on an ice bath (0° C.), which was stirred for 30 minutes at room temperature. 2-Fluoro-6-methylpyridine (1.8 g, 16.2 mmol) was then added to the reaction mixture on an ice bath (0° C.), and stirred for 5 hours at room temperature. The reaction mixture was partitioned into water and ethyl acetate on the ice bath (0° C.). The organic layer was washed with water and saturated aqueous sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:15) to obtain the title compound (3.65 g, 81%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841327B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-4ca960c85e344d46bd981f40a03e059c
출처 메모uspto-grants-2014_09