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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15030생성일: 2026년 10월 23일

Acetic Anhydride → 4-Benzyloxy-2(1H)-pyridone

https://huagongshe.com/ko/reaction/15030

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물4-(Benzyloxy)pyridine N-oxideHCID 295871—
생성물4-Benzyloxy-2(1H)-pyridoneHCID 360772449%

반응 단계

4-Benzyloxypyridine 1-oxide (24.8 g, 123 mmols) was refluxed in acetic anhydride (150 mL) for 1.5 hours. Cooling the system to room temperature, the system was concentrated under reduced pressure and the resulting residue was dissolved in a mixed solvent of ethyl acetate (150 mL) and methanol (10 mL), followed by stirring at 60° C. for 2 hours. The solid formed upon cooling the system to room temperature was recovered by filtration to provide crude title compound (8.84 g). Concentrating the filtrate, additional crude title compound (4.17 g) was obtained. The combined crude product was recrystallized from a mixed solvent of methanol and ethyl acetate to provide the title compound (12.1 g, 49%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732456B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-49d140b0dab5425e960646c5242341e6
출처 메모uspto-grants-2010_06