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HRID 244938作成日:2026年10月26日

Pyridine → Ethyl 4,4-dimethyl-3-oxo-5-phenylpentanoate

https://huagongshe.com/reaction/244938

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Ethyl AcetoacetateHCID 8868—
反応物Magnesium ChlorideHCID 5360315—
反応物2,2-Dimethyl-3-phenylpropanoyl chlorideHCID 13307229—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 4,4-dimethyl-3-oxo-5-phenylpentanoateHCID 8669746018%

反応条件

温度0 °C

反応手順

Ethyl 3-oxobutanoate (1.09 g, 8.3 mmol) in methylene chloride (16 mL) was mixed with anhydrous magnesium chloride (158 mg, 1.66 mmol), and the reaction solution was cooled to 0° C., mixed with pyridine (1.34 mL, 16.6 mmol), stirred for 30 minutes, then mixed with 2,2-dimethyl-3-phenylpropanoyl chloride (1.64 g, 8.3 mmol) and stirred for another 30 minutes at the same temperature. The reaction solution was warmed to room temperature and stirred for 20 hours. The methylene chloride was distilled off under reduced pressure, and the residue was with ethanol (2 mL) and at room temperature for 2 days and with toluene (2 mL) at 60° C. for 5 hours. After completion of the reaction, the reaction solution was washed with saturated aqueous sodium hydrogen carbonate and extracted with ethyl acetate (50 mL×2). The solvent was removed from the resulting organic layer under reduced pressure, and the resulting brown oil was purified by intermediate pressure silica gel column chromatography (silica gel12 g, ethyl acetate:hexane=1:19 to 1:9) to give 370 mg of the desired product as a light brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08658686B2
出典データセットuspto-grants-2014_02
ORD IDord-f310f4dcb6274a00b1d15af426616c40
出典メモuspto-grants-2014_02