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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1725181생성일: 2026년 10월 26일

Sulfuric Acid → 2-(4-Propyl-cyclohexanecarbonyl)-malonic acid diethyl ester

https://huagongshe.com/reaction/1725181

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물Diethyl MalonateHCID 7761—
반응물MagnesiumHCID 5462224—
반응물Cyclohexanecarbonyl chloride, 4-propyl-, trans-HCID 12780024—
용매EthanolHCID 702—
용매TolueneHCID 1140—
용매Carbon TetrachlorideHCID 5943—
용매Sodium chloride; waterHCID 57417360—
생성물2-(4-Propyl-cyclohexanecarbonyl)-malonic acid diethyl esterHCID 6905998068.6%

반응 단계

To 2.5 mL of anhydrous EtOH and 0.25 mL carbon tetrachloride was added 1.2 g (50 mmol) magnesium turnings. 8.0 g (50 mmol) diethyl malonate was dissolved in a mixture of 5 mL anhydrous EtOH and 20 mL anhydrous toluene and added in small portions to the magnesium turnings over the course of 1.5 hr so as to maintain a gentle reflux. The reaction was stirred at room temperature for 1 hr, and then cooled to 0° C. in ice. 4-Propyl-cyclohexanecarbonyl chloride (50 mmol) was added dropwise and the reaction was allowed to warm to room temperature over night. The reaction was then heated to 55° C. for 4 hr with stirring, allowed to cool to ambient temperature, and was poured into a slurry of crushed ice and 10% H2SO4. The solution was diluted with brine and extracted with ethyl acetate. The organic layer was separated, dried over MgSO4, and concentrated to afford 10.71 g (34.28 mmol) 2-(4-propyl-cyclohexanecarbonyl)-malonic acid diethyl ester as a clear, near colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07488832B2
출처 데이터셋uspto-grants-2009_02
ORD IDord-44c439965f4b4537b0c76da3e33c7e09
출처 메모uspto-grants-2009_02