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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15029생성일: 2026년 10월 24일

Benzyl Alcohol → 4-(Benzyloxy)pyridine N-oxide

https://huagongshe.com/ko/reaction/15029

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl AlcoholHCID 244—
반응물4-Nitropyridine N-oxideHCID 14300—
반응물Sodium hydrideHCID 24758—
용매DimethylformamideHCID 6228—
생성물4-(Benzyloxy)pyridine N-oxideHCID 29587169%

반응 단계

To a DMF suspension (200 mL) of sodium hydride (60% oilyness, 7.50 g, 0.188 mmol), benzyl alcohol (20.3 mL) was added under cooling with ice, and stirred for an hour at room temperature. Then 4-nitropyridine 1-oxide (25.5 g, 182 mmols) was added little by little under stirring, followed by an hour's stirring at room temperature. The solvent was concentrated under reduced pressure and chloroform (1 L) was added to the resulting residue. The insoluble matter was filtered using Celite (100 g). The filtrate was concentrated and to which acetone was added to provide the title compound (24.8 g, 69%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732456B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c43af34c914f4fb79783195755e66732
출처 메모uspto-grants-2010_06