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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 244938생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/244938

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Ethyl AcetoacetateHCID 8868—
반응물Magnesium ChlorideHCID 5360315—
반응물2,2-Dimethyl-3-phenylpropanoyl chlorideHCID 13307229—
용매DichloromethaneHCID 6344—
생성물Ethyl 4,4-dimethyl-3-oxo-5-phenylpentanoateHCID 8669746018%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658686B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-f310f4dcb6274a00b1d15af426616c40
출처 메모uspto-grants-2014_02