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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 856683생성일: 2026년 10월 25일

4-Nitropyridine N-oxide → 4-Ethoxypyridine n-oxide

https://huagongshe.com/reaction/856683

반응식

참여 물질

역할이름HCID투입량
반응물4-Nitropyridine N-oxideHCID 14300—
반응물Sodium ethoxideHCID 2723922—
용매EthanolHCID 702—
생성물4-Ethoxypyridine n-oxideHCID 25247999%

반응 조건

온도50 °C

반응 단계

4-nitropyridine-N-oxide (12 g) was dissolved in ethanol, sodium ethoxide (8.8 g) was added to the mixture, and the mixture was stirred for 40 hours at 50° C. After allowing the mixture to be cooled to room temperature, the precipitates were filtered, the solvent was removed under reduced pressure, and the obtained residue was purified by silica gel column chromatography, to give 4-ethoxypyridine-N-oxide (11.8 g). To 4-ethoxypyridine-N-oxide (11.8 g) was added dimethyl sulfate (8.56 ml), and the mixture was stirred for 1 hour at 110° C. After diluting with methanol (180 ml), the mixture was heated to reflux for 1 hour, an aqueous solution (18 ml) of ammonium peroxodisulfate (20.6 g) was added dropwise to the solution under heat reflux, and the mixture was heated to reflux for 1 hour. After allowing the mixture to be cooled to room temperature, the solvent was removed under reduced pressure, and the obtained residue was purified by silica gel column chromatography, to give (4-ethoxy-2-pyridinyl)methanol (2.8 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07262185B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-ea5cc24d7f8e45ab98589abaa1ff7bc6
출처 메모uspto-grants-2007_08