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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1820852생성일: 2026년 10월 27일

4-Acetylbiphenyl → Ethyl 3-oxo-3-(4-phenylphenyl)propanoate

https://huagongshe.com/reaction/1820852

반응식

참여 물질

역할이름HCID투입량
반응물4-AcetylbiphenylHCID 7113—
반응물Diethyl CarbonateHCID 7766—
반응물Sodium hydrideHCID 24758—
생성물Ethyl 3-oxo-3-(4-phenylphenyl)propanoateHCID 2756708—

반응 조건

온도80 °C

반응 단계

14.7 g (75.0 mmol) of 4-acetylbiphenyl is dissolved in 150 mL of diethylcarbonate. Under protective gas, a total of 6.50 g (150 mmol) sodium hydride in oil (55%) is added batchwise at 0° C. The mixture is kept for 5 minutes at 0° C., then stirred for 2 hours at 80° C. After cooling, the mixture is poured onto water and extracted with methylene chloride; the organic phase is washed with water and finally dried over sodium sulfate. The solvent is eliminated, the residue is suspended in water and neutralized with 1N hydrochloric acid. The aqueous phase is extracted with diethyl ether, the organic phase is dried over sodium sulfate, and finally the solvent is eliminated. Lastly the residue is recrystallized from petroleum ether and the product is dried in vacuo at 50° C. Yield: 15.3 g (76% of theory); Rf value: 0.60 (silica gel, petroleum ether/ethyl acetate=5:2); m.p. 75° C.-77° C.; C17H16O3; EII mass spectrum: m/z=269 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07605176B2
출처 데이터셋uspto-grants-2009_10
ORD IDord-c178a8d09327411d82e92ac88faa8d7a
출처 메모uspto-grants-2009_10