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HRID 1645417생성일: 2026년 10월 26일

Pyridine → Ethyl 4-(4-fluorophenyl)-3-oxobutanoate

https://huagongshe.com/reaction/1645417

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
반응물4-Fluorophenylacetyl chlorideHCID 3744988—
반응물5-(4-Fluorophenyl)-4-oxo-1,4-dihydropyridine-3-carboxylic acidHCID 60204207—
용매EthanolHCID 702—
생성물Ethyl 4-(4-fluorophenyl)-3-oxobutanoateHCID 10585213—

반응 단계

The intermediate, 5-(4-fluorophenyl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid (8) can be obtained using the chemistry described in Scheme 2. Thus, 2-(4-fluorophenyl)acetyl chloride (10) can be treated with 2,2-dimethyl-1,3-dioxane-4,6-dione (Meldrum's acid) in the presence of pyridine and the resulting adduct can be refluxed in ethanol to afford ethyl 4-(4-fluorophenyl)-3-oxobutanoate (12). Treatment of intermediate 12 with triazine and sodium ethoxide in ethanol can furnish the requisite ester intermediate, which can be readily hydrolyzed in the presence of sodium hydroxide at elevated temperature to furnish intermediate 8.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08124768B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-0d5cdb20972546f3bf686e133ee32594
출처 메모uspto-grants-2012_02