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HRID 31612생성일: 2026년 10월 26일

2,3,5-Trimethylpyridine → 2,3,5-Trimethyl-1-oxidopyridin-1-ium

https://huagongshe.com/reaction/31612

반응식

참여 물질

역할이름HCID투입량
반응물2,3,5-TrimethylpyridineHCID 12759—
반응물m-Chloroperbenzoic acidHCID 70297—
용매DichloromethaneHCID 6344—
생성물2,3,5-Trimethyl-1-oxidopyridin-1-iumHCID 10486907—

반응 단계

To a dichloromethane (dehydrated) (150 ml) solution of a 2,3,5-collidine (11.0 g, 90.8 mmol), 3-chloroperbenzoic acid (24.8 g, 93.4 mmol as the content was regarded as 65%) was added at 1° C. in a nitrogen atmosphere. The mixture was stirred while the temperature was gradually raised to room temperature for 13.5 hours. After the reaction mixture was concentrated, the residue was purified by silica gel column chromatography (NH silica gel: 200 g, elution solvent: heptane/ethyl acetate=50/50, ethyl acetate, ethyl acetate/methanol=20/1) to obtain a crude product of the title compound as a pale yellow oil. After the crude product was diluted with ethyl acetate and a saturated aqueous solution of sodium hydrogen carbonate, the mixture was concentrated. The residue was purified by silica gel column chromatography (NH silica gel: 300 g, elution solvent: heptane, heptane/ethyl acetate=50/50, ethyl acetate, ethyl acetate/methanol=20/1) to obtain the title compound (11.0 g, yield: 88.3%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425634B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-b2f12b68d49e437499c46a80f630ba27
출처 메모uspto-grants-2008_09