戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 541149作成日:2026年10月25日

Citric Acid → 2-(5-Methoxy-pyridin-2-yl)-benzoic acid diethylamide

https://huagongshe.com/reaction/541149

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Potassium Phosphate, TribasicHCID 62657—
反応物(2-(Diethylcarbamoyl)phenyl)boronic acidHCID 4190636—
反応物2-Chloro-5-methoxypyridineHCID 15169000—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物2-(5-Methoxy-pyridin-2-yl)-benzoic acid diethylamideHCID 5949278728.2%

反応条件

温度80 °C

反応手順

Under an argon atmosphere, a mixture of tripotassium phosphate (6.24 g) and water (15 ml) was added to a mixture of 2-chloro-5-methoxy-pyridine (2.05 g), 2-(diethylcarbamoyl)benzeneboronic acid (4.65 g), 1,1′-bis(diphenylphosphino)ferrocene-palladium(II) dichloride-dichloromethane complex (0.584 g) and toluene (30 ml), and the mixture was stirred at 80° C. for 2 hr. The reaction mixture was cooled to room temperature, water (20 ml), citric acid (2.2 g) and ethyl acetate were added and the mixture was stirred and filtered through celite. The filtrate was partitioned in a separatory funnel. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure and the obtained residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=1/1 to 1/2) to give a roughly purified product (1.144 g) of the title compound. This product was directly used for the next reaction without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08871934B2
出典データセットuspto-grants-2014_10
ORD IDord-996e065bbc964b5c82d86c73e3dba0a9
出典メモuspto-grants-2014_10