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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 591818생성일: 2026년 10월 26일

2,6-Dimethylpyridine N-oxide → 2,6-Dimethyl-4-(hydroxymethyl)pyridine

https://huagongshe.com/reaction/591818

반응식

참여 물질

역할이름HCID투입량
반응물2,6-Dimethylpyridine N-oxideHCID 14083—
반응물Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1)HCID 2735153—
용매DichloromethaneHCID 6344—
생성물2,6-Dimethyl-4-(hydroxymethyl)pyridineHCID 3825077168.7%

반응 단계

A solution of 2,6-lutidine N-oxide (41.6 g, 0.337 mol, 1.0 equiv.) in dry DCM (650 mL) was added to a flask containing trimethyloxonium tetrafluoroborate (50.0 g, 0.337 mol, 1.0 equiv.) at room temperature. under a nitrogen atmosphere. The mixture was stirred at room temperature for 3.0 hours, then concentrated in vacuo to give 78 g of crude 4-hydroxymethyl-2,6-dimethylpyridine. The crude product was dissolved in methanol (500 mL) and the solution was heated to reflux under a nitrogen atmosphere, then a solution of ammonium persulfate (24.6 g, 0.101 mol) in water (100 mL) was added dropwise. The mixture was stirred at reflux for 16 hours; TLC indicated complete reaction. Half of the solvents were removed in vacuo, then quenched with 10% NaOH solution to pH approximately 7, and evaporated to dryness. The residue was dissolved in methanol and filtered, the filtrate was concentrated in vacuum, and purified by column chromatography (eluting with methanol: DCM=5-15%) to give the title compound as a white solid. Yield: 24.7 g (52%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09238640B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-10523c9ad4bb4b6594fcea8c9eb51f1b
출처 메모uspto-grants-2016_01