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HRID 273397作成日:2026年10月26日

Citric Acid → 3-(4-{[2'-Methyl-4'-(3-(pyridin-2-yl)propoxy)biphenyl-3-yl]methoxy}phenyl)propanoic acid

https://huagongshe.com/reaction/273397

反応式

関与物質

役割名称HCID仕込み量
反応物Citric AcidHCID 311—
反応物WaterHCID 962—
反応物Sodium HydroxideHCID 14798—
反応物Methyl 3-(4-{[2'-methyl-4'-(3-(pyridin-2-yl)propoxy)biphenyl-3-yl]methoxy}phenyl)propanoateHCID 58903135—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物3-(4-{[2'-Methyl-4'-(3-(pyridin-2-yl)propoxy)biphenyl-3-yl]methoxy}phenyl)propanoic acidHCID 5890315748%

反応手順

A solution of methyl 3-(4-{[2′-methyl-4′-(3-(pyridin-2-yl)propoxy)biphenyl-3-yl]methoxy}phenyl)propanoate (0.401 g, 0.809 mmol) in methanol (5 mL) and tetrahydrofuran (5 mL) was added 2 M aqueous sodium hydroxide solution (1.5 mL) and the mixture was stirred at room temperature for 75 hrs. Water was added to the reaction mixture, and the mixture was neutralized with 10% aqueous citric acid solution and extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (50% ethyl acetate/hexane-ethyl acetate) and recrystallized from ethyl acetate-hexane to give the title compound (0.186 g, yield 48%) as colorless prism crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07456218B2
出典データセットuspto-grants-2008_11
ORD IDord-7a1bdf52ca2f4b0b97a84b6b303cd15e
出典メモuspto-grants-2008_11