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HRID 341675생성일: 2026년 10월 26일

Hydrochloric Acid → 6-(3,5-Dimethylbiphenyl-4-yl)-2,2,4,4-tetramethylcyclohexane-1,3,5-trione

https://huagongshe.com/reaction/341675

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TolueneHCID 1140—
반응물ChloroformHCID 6212—
반응물3,5-Dioxohexanoic acidHCID 5459844—
반응물2,2,4,4-Tetramethylcyclohexane-1,3,5-trioneHCID 11769166—
촉매4-(Dimethylamino)pyridineHCID 14284—
생성물6-(3,5-Dimethylbiphenyl-4-yl)-2,2,4,4-tetramethylcyclohexane-1,3,5-trioneHCID 68732214—

반응 단계

To a mixture of 2,2,4,4-tetramethylcyclohexane-1,3,5-trione (182 mg, 1 mmol) and 4-dimethylaminopyridine (610 mg, 5 mmol) under an atmosphere of nitrogen, is added dry chloroform (5.6 ml), followed by stirring at room temperature until dissolution is complete. To this solution is then added dry toluene (2 ml), and 3,5-dimethylbiphenylead triacetate (0.5 M solution in dry chloroform, 2.4 ml, 1.2 mmol). This solution is then heated under reflux for 1 hour. The reaction mixture is cooled to room temperature, acidified to pH 1 with 2N aqueous hydrochloric acid, filtered and the filtrate is extracted with dichloromethane (2×40 ml). The organic extracts are combined, dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated under reduced pressure. The residue is further purified by column chromatography on silica gel to give 6-(3,5-dimethylbiphenyl-4-yl)-2,2,4,4-tetramethylcyclohexane-1,3,5-trione (166 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895761B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-bca18a6890a54f3aab0a2c733f23c31a
출처 메모uspto-grants-2014_11