戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2389910作成日:2026年10月27日

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

https://huagongshe.com/reaction/2389910

反応式

関与物質

役割名称HCID仕込み量
反応物Maleic AnhydrideHCID 7923—
反応物Hydrochloride methanolHCID 21893726—
反応物trimethylsilyldiazomethane Et2OHCID 23159941—
反応物Methyl 3-(5-ethoxy-1,3-oxazol-2-yl)propanoateHCID 59179423—
生成物Dimethyl 5-hydroxy-2-(3-methoxy-3-oxopropyl)pyridine-3,4-dicarboxylateHCID 5917939830%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08273761B2
出典データセットuspto-grants-2012_09
ORD IDord-d42a55341dc3431886b22fc9a9422f29
出典メモuspto-grants-2012_09