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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40630생성일: 2026년 10월 23일

2-Methyl-5-hydroxypyridine → (S)-2-Methyl-5-oxiranylmethoxy-pyridine

https://huagongshe.com/ko/reaction/40630

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-5-hydroxypyridineHCID 14275—
반응물Sodium hydrideHCID 24758—
반응물Benzenesulfonic acid, 3-nitro-, (2S)-2-oxiranylmethyl esterHCID 146490—
용매DimethylformamideHCID 6228—
생성물(S)-2-Methyl-5-oxiranylmethoxy-pyridineHCID 59686824—

반응 단계

6-Methyl-pyridin-3-ol (0.218 g, 2.0 mmol) was placed in a flask with DMF (10 mL) and NaH (60% dispersion in oil, 77 mg, 2.0 mmol) and stirred for 30 min. at room temperature. (S)-glycidyl 3-nitrobenzene sulfonate (0.52 g, 2.0 mmol) was then added to the reaction mixture, which was then stirred at room temperature for 14 hours. The reaction was quenched with NaHCO3 (saturated) and then extracted three times with ethyl acetate. The organic layer was dried with magnesium sulfate, filtered and the solvent was evaporated under reduced pressure to yield crude product which was purified by silica gel chromatography (60% Ethyl acetate/heptane) to yield the title compound as a residue.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530475B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-9bf078de8aa64806aabfd30258c40a4a
출처 메모uspto-grants-2013_09