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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1725183생성일: 2026년 10월 26일

Phenacyl bromide → 4-Oxo-4-phenyl-2-(4-propyl-cyclohexanecarbonyl)-butyric acid ethyl ester

https://huagongshe.com/reaction/1725183

반응식

참여 물질

역할이름HCID투입량
반응물Phenacyl bromideHCID 6259—
반응물Sodium hydrideHCID 24758—
반응물3-Oxo-3-(4-propyl-cyclohexyl)-propionic acid ethyl esterHCID 57423720—
용매TetrahydrofuranHCID 8028—
용매Sodium chloride; waterHCID 57417360—
생성물4-Oxo-4-phenyl-2-(4-propyl-cyclohexanecarbonyl)-butyric acid ethyl esterHCID 69061689115.5%

반응 조건

온도0 °C

반응 단계

To a stirred slurry of 0.92 g (23 mmol) NaH, 60% dispersion in mineral oil, in 30 mL anhydrous THF, cooled 0° C. in ice, 5.12 g (21.3 mmol) 3-oxo-3-(4-propyl-cyclohexyl)-propionic acid ethyl ester from Step 2 was added dropwise over the course of 60 min. The reaction was stirred at 0° C. for 1 hr. 2-bromoacetophenone (5.57 g, 28 mmol) in 12 mL anhydrous THF was then added dropwise at 0° C. and the reaction was allowed to stir at room temperature over 5 days. The reaction was poured into brine, extracted with ethyl acetate, dried over MgSO4, and concentrated to afford 8.85 g (24.6 mmol, 115% yield) 4-oxo-4-phenyl-2-(4-propyl-cyclohexanecarbonyl)-butyric acid ethyl ester as an oil. The product was used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07488832B2
출처 데이터셋uspto-grants-2009_02
ORD IDord-94058aeecafe4b6dbe3f7ec07bb88595
출처 메모uspto-grants-2009_02