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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2389910생성일: 2026년 10월 26일

Maleic Anhydride → Dimethyl 5-hydroxy-2-(3-methoxy-3-oxopropyl)pyridine-3,4-dicarboxylate

https://huagongshe.com/reaction/2389910

반응식

참여 물질

역할이름HCID투입량
반응물Maleic AnhydrideHCID 7923—
반응물Hydrochloride methanolHCID 21893726—
반응물trimethylsilyldiazomethane Et2OHCID 23159941—
반응물Methyl 3-(5-ethoxy-1,3-oxazol-2-yl)propanoateHCID 59179423—
생성물Dimethyl 5-hydroxy-2-(3-methoxy-3-oxopropyl)pyridine-3,4-dicarboxylateHCID 5917939830%

반응 단계

A mixture of methyl 3-(5-ethoxy-1,3-oxazol-2-yl)propanoate (7.00 g, 35.1 mmol) and maleic anhydride (3.44 g, 35.1 mmol) was stirred at room temperature for 2 hr, 10% hydrochloric acid-methanol solution (100 mL) was added, and the mixture was heated under reflux for 15 hr. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/methanol=100/0→70/30). The purified product was dissolved in methanol, 2M trimethylsilyldiazomethane/diethyl ether solution (34 mL, 68 mmol) was added at room temperature, and the mixture was stirred for 30 min. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=25/75→50/50) to give the title compound (3.10 g, yield 30%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08273761B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-d42a55341dc3431886b22fc9a9422f29
출처 메모uspto-grants-2012_09